Pub Date : 2023-01-01DOI: 10.4103/jasi.jasi_144_21
M. Sindel, Serra Ozturk, Güneş Aytaç, A. Karadas, Betul Danısman, G. Tanriover, N. Derin, G. Akkoyunlu, F. Kızılay
{"title":"Demonstration of the decrease in locomotor activity and central nervous system in the demyelination model, in which the toxic agent is realized by gavage","authors":"M. Sindel, Serra Ozturk, Güneş Aytaç, A. Karadas, Betul Danısman, G. Tanriover, N. Derin, G. Akkoyunlu, F. Kızılay","doi":"10.4103/jasi.jasi_144_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_144_21","url":null,"abstract":"","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70780907","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Students' approaches to learning anatomy: The road to better teaching and learning","authors":"Mohamed Al Mushaiqri, Adnan Albaloshi, Srijit Das","doi":"10.4103/jasi.jasi_67_22","DOIUrl":"https://doi.org/10.4103/jasi.jasi_67_22","url":null,"abstract":"","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70782174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-01-01DOI: 10.4103/jasi.jasi_106_21
{"title":"A rare aortic arch anomaly: Combination of vertebral arteria lusoria with Kommerell's diverticulum, bovine aortic arch, and left vertebral artery with extreme proximal origin","authors":"","doi":"10.4103/jasi.jasi_106_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_106_21","url":null,"abstract":"","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70780841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"An alternative route for petroclival tumors: Without mastoidectomy and superior petrosal sinus ligation: A cadaveric study","authors":"A. Başak, M. Özbek","doi":"10.4103/jasi.jasi_18_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_18_21","url":null,"abstract":"","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70781065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-01-01DOI: 10.4103/jasi.jasi_186_21
B. Candan, E. Torun, Rumeysa Dikici, S. Avnioglu, MehmetYalcin Gunal
{"title":"Correlation of some anatomical angles of the shoulder with rotator cuff syndrome","authors":"B. Candan, E. Torun, Rumeysa Dikici, S. Avnioglu, MehmetYalcin Gunal","doi":"10.4103/jasi.jasi_186_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_186_21","url":null,"abstract":"","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70781117","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Persistent left superior vena cava (PLSVC) is uncommon with an incidence of 0.3%–1.3%. The incidence of absent papillary muscle is unknown. Congenital anomalies of a thoracic venous system associated with absent papillary muscle are very rare. During dissection of a 55-year-old male cadaver, PLSVC with absent papillary muscle was found. Although these congenital anomalies are incidentally found, it is worthwhile following such patients to look for the evolution of any cardiac symptoms. Sound knowledge and awareness of such congenital anomalies are required for radiologists, cardiothoracic surgeons, and critical care physicians.
{"title":"Case report of persistent left superior vena cava with absent papillary muscle – Unusual coexistence","authors":"Divya Umamaheswaran, Jayagandhi Sakkarai, Rema Devi","doi":"10.4103/jasi.jasi_81_22","DOIUrl":"https://doi.org/10.4103/jasi.jasi_81_22","url":null,"abstract":"Persistent left superior vena cava (PLSVC) is uncommon with an incidence of 0.3%–1.3%. The incidence of absent papillary muscle is unknown. Congenital anomalies of a thoracic venous system associated with absent papillary muscle are very rare. During dissection of a 55-year-old male cadaver, PLSVC with absent papillary muscle was found. Although these congenital anomalies are incidentally found, it is worthwhile following such patients to look for the evolution of any cardiac symptoms. Sound knowledge and awareness of such congenital anomalies are required for radiologists, cardiothoracic surgeons, and critical care physicians.","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"71 1","pages":"324 - 328"},"PeriodicalIF":0.4,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49027710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Interpretation of traumatological radiographs of the region of the elbow joint may come with many challenges. Aside from traumatological avulsions and fractures, we can also identify other entities such as persistent epiphysis, aseptic necrosis, osteochondritis dissecans, calcific bursitis, synovial chondromatosis, and other degenerative changes. It is also necessary for all these pathological conditions to be differentiated from the anatomical variants. Material and Methods: We performed a retrospective analysis of patients admitted to our clinic between 2010 and 2020 for arthroscopic treatment of chronic elbow joint stiffness. We evaluated the radiographs of their elbow joints for the presence of accessory ossification. If present, these cases were then sorted by previously defined criteria into groups according to the kind of anatomical variant and degenerative changes. On the basis of these data, we performed a statistical analysis. Results: We analyzed 39 limbs in 39 patients (12 women and 27 men). The average age was 40.9 years (span 16–74). The exclusion criteria did not exclude any patient. Accessory ossifications were present in 78.4% (29/37) of patients, and all three criteria for accessory bone were fulfilled by two patients. Discussion and Conclusion: This sample of patients suffering from joint stiffness due to degenerative changes around the elbow joint enabled us to prove the usefulness of the criteria for differentiating degenerative changes from accessory bones. We were also able to validate the hypothesis that in a sample of patients suffering from elbow stiffness, the dominant cause of the stiffness should be the degenerative changes, while the accessory bones prevalence should not differ significantly from their prevalence in the healthy population. Our analysis showed that the seemingly ovoid intra-articular loose bodies do not appear on the radiographs as regularly shaped and can be differentiated from accessory bones. In order to avoid the wrong interpretation of elbow radiographs, it is necessary to be aware of this issue. Our study validates the three previously defined criteria as means to diagnose accessory bones with a high specificity. The intra-articular loose bodies macroscopically seemed ovoid and regular. Nevertheless, they do not appear as regularly shaped on radiographs and do not, therefore, fulfill the criteria of accessory bones.
{"title":"Ambiguity of the radiographs around the elbow joint: Anatomical variant versus degenerative changes","authors":"V. Kunc, V. Kunc, K. Kuncová, D. Kachlík, L. Kopp","doi":"10.4103/jasi.jasi_80_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_80_21","url":null,"abstract":"Introduction: Interpretation of traumatological radiographs of the region of the elbow joint may come with many challenges. Aside from traumatological avulsions and fractures, we can also identify other entities such as persistent epiphysis, aseptic necrosis, osteochondritis dissecans, calcific bursitis, synovial chondromatosis, and other degenerative changes. It is also necessary for all these pathological conditions to be differentiated from the anatomical variants. Material and Methods: We performed a retrospective analysis of patients admitted to our clinic between 2010 and 2020 for arthroscopic treatment of chronic elbow joint stiffness. We evaluated the radiographs of their elbow joints for the presence of accessory ossification. If present, these cases were then sorted by previously defined criteria into groups according to the kind of anatomical variant and degenerative changes. On the basis of these data, we performed a statistical analysis. Results: We analyzed 39 limbs in 39 patients (12 women and 27 men). The average age was 40.9 years (span 16–74). The exclusion criteria did not exclude any patient. Accessory ossifications were present in 78.4% (29/37) of patients, and all three criteria for accessory bone were fulfilled by two patients. Discussion and Conclusion: This sample of patients suffering from joint stiffness due to degenerative changes around the elbow joint enabled us to prove the usefulness of the criteria for differentiating degenerative changes from accessory bones. We were also able to validate the hypothesis that in a sample of patients suffering from elbow stiffness, the dominant cause of the stiffness should be the degenerative changes, while the accessory bones prevalence should not differ significantly from their prevalence in the healthy population. Our analysis showed that the seemingly ovoid intra-articular loose bodies do not appear on the radiographs as regularly shaped and can be differentiated from accessory bones. In order to avoid the wrong interpretation of elbow radiographs, it is necessary to be aware of this issue. Our study validates the three previously defined criteria as means to diagnose accessory bones with a high specificity. The intra-articular loose bodies macroscopically seemed ovoid and regular. Nevertheless, they do not appear as regularly shaped on radiographs and do not, therefore, fulfill the criteria of accessory bones.","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"71 1","pages":"303 - 306"},"PeriodicalIF":0.4,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49314884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-10-01DOI: 10.4103/jasi.jasi_182_21
K. Sharma, Rishita Chandra, Brijendra Singh, Shashi Mani Yadav, Manisha Naithani, S. Kishore, Vivek Mishra, K. Mohan, P. Verma
Introduction: Familial Short stature is considered one of the most common causes of Short Stature along with the constitutional delay in growth and puberty (CDGP) from which it can easily be distinguish. The core parameters of anthropometry represent diagnostic criteria for obesity and other non-communicable diseases. To measure the anthropometric parameters in the patients with idiopathic clinically non-syndromic familial short-stature and to correlate those parameters with their height and compare them with the control group. Material and Methods: A cross-sectional study was conducted among Familial Short Stature females of 5-18 years age group referred from Paediatric and Genetic OPD of AIIMS, Rishkesh. Non-parametric tests were applied for comparing the variables and correlation coefficients were obtained. Results: There was a significant difference between the groups in terms of Standing Height (cm) (W = 376.000, P = <0.001), BMI (Kg/m2) (W = 1128.500, P = 0.002), with the median BMI (Kg/m2) and Waist/Height Ratio (W = 1164.500, P = <0.001), with the median Waist/Height Ratio being highest in the Short-Stature group. There was moderate to strong positive correlation between standing height and other anthropometric parameters. The mean waist to height ratio of 0.6 among short stature and 0.5 among the control group, with short stature having more odds of getting overweight and also shows a greater predilection of short-stature group for developing Cardio-vascular diseases. Discussion and Conclusion: Familial short stature though being a manifestation of some underlying cause, can fall in a non-syndromic group until further studies including karyotyping, next-generation sequencing etc. Extensive research for appropriate categorization and how this can effectively help combat the burden of malnutrition and non-communicable diseases should be done.
家族性身材矮小被认为是矮小的最常见的原因之一，它与生长发育和青春期的体质延迟(CDGP)很容易区分。人体测量学的核心参数是肥胖症和其他非传染性疾病的诊断标准。目的测定特发性临床非综合征性家族性矮小患者的人体测量参数，并将这些参数与身高进行相关性分析，并与对照组进行比较。材料和方法:对来自瑞什凯什AIIMS儿科和遗传OPD的5-18岁的家族矮小女性进行了横断面研究。采用非参数检验对各变量进行比较，得到相关系数。结果:两组患者站高(cm) (W = 376.000, P = <0.001)、体重指数(Kg/m2) (W = 1128.500, P = 0.002)、中位BMI (Kg/m2)和腰高比(W = 1164.500, P = <0.001)差异均有统计学意义，其中矮身材组腰高比中位最高。站立高度与其他人体测量参数呈正相关。矮个子组的平均腰高比为0.6，对照组的平均腰高比为0.5，矮个子组肥胖的几率更高，也更容易患心血管疾病。讨论与结论:家族性身材矮小虽然是某种潜在原因的表现，但也可能属于非综合征组，需要进一步的研究，包括核型分析、下一代测序等。应该进行广泛的研究，以便进行适当的分类，以及如何有效地帮助消除营养不良和非传染性疾病的负担。
{"title":"Anthropometric parameters of idiopathic familial short stature females and its correlation with height and comparison with the control group","authors":"K. Sharma, Rishita Chandra, Brijendra Singh, Shashi Mani Yadav, Manisha Naithani, S. Kishore, Vivek Mishra, K. Mohan, P. Verma","doi":"10.4103/jasi.jasi_182_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_182_21","url":null,"abstract":"Introduction: Familial Short stature is considered one of the most common causes of Short Stature along with the constitutional delay in growth and puberty (CDGP) from which it can easily be distinguish. The core parameters of anthropometry represent diagnostic criteria for obesity and other non-communicable diseases. To measure the anthropometric parameters in the patients with idiopathic clinically non-syndromic familial short-stature and to correlate those parameters with their height and compare them with the control group. Material and Methods: A cross-sectional study was conducted among Familial Short Stature females of 5-18 years age group referred from Paediatric and Genetic OPD of AIIMS, Rishkesh. Non-parametric tests were applied for comparing the variables and correlation coefficients were obtained. Results: There was a significant difference between the groups in terms of Standing Height (cm) (W = 376.000, P = <0.001), BMI (Kg/m2) (W = 1128.500, P = 0.002), with the median BMI (Kg/m2) and Waist/Height Ratio (W = 1164.500, P = <0.001), with the median Waist/Height Ratio being highest in the Short-Stature group. There was moderate to strong positive correlation between standing height and other anthropometric parameters. The mean waist to height ratio of 0.6 among short stature and 0.5 among the control group, with short stature having more odds of getting overweight and also shows a greater predilection of short-stature group for developing Cardio-vascular diseases. Discussion and Conclusion: Familial short stature though being a manifestation of some underlying cause, can fall in a non-syndromic group until further studies including karyotyping, next-generation sequencing etc. Extensive research for appropriate categorization and how this can effectively help combat the burden of malnutrition and non-communicable diseases should be done.","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"71 1","pages":"288 - 294"},"PeriodicalIF":0.4,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46397234","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Alterations in chromosome number have a strong impact on outcome in childhood ALL. Genetic findings may predict the prognosis and biologic properties of the leukemia more consistently than does morphology. To see the numerical aberrations in ALL in North Indian population Material and Methods: Culture and chromosome banding of bone marrow and blood sample of 51 North Indian patients of ALL (44 males and 7 females) from the age group of 2 to 42 years were done. Only 39 shows good chromosomal spread, so 39 karyograms were prepared and observed for the chromosomal gain or loss and their frequency. Results: Numerical abnormalities were observed in 14 patients (35.9%) of the 39 cytogenetically analysed cases. Trisomy 21 was found in 3 cases. Trisomy of chromosome number 13 and 14 were found in 5.12% cases. Trisomy of chromosome number 3, 4, 6, 8, 11, 15, 17 and 18 were present in 2.56% cases (Fig. 21, 30, 31, 34, 35, 42). Gain of chromosome X was seen in 5.12% cases while only in one case (2.56%) gain of chromosome Y was detected. Discussion and Conclusion: Numerical chromosomal abnormality in this study was 15.38% which was different from other population described in previous studies. Trisomy 21 is most common in this study. The findings of the present study may be useful for the clinician in predicting outcome, remission, survival and treatment response in ALL.
{"title":"Numerical chromosomal aberrations in acute lymphoblastic leukemia in North Indians","authors":"Indu Shri, R. Verma, A. Rani, Navneet Kumar","doi":"10.4103/jasi.jasi_97_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_97_21","url":null,"abstract":"Introduction: Alterations in chromosome number have a strong impact on outcome in childhood ALL. Genetic findings may predict the prognosis and biologic properties of the leukemia more consistently than does morphology. To see the numerical aberrations in ALL in North Indian population Material and Methods: Culture and chromosome banding of bone marrow and blood sample of 51 North Indian patients of ALL (44 males and 7 females) from the age group of 2 to 42 years were done. Only 39 shows good chromosomal spread, so 39 karyograms were prepared and observed for the chromosomal gain or loss and their frequency. Results: Numerical abnormalities were observed in 14 patients (35.9%) of the 39 cytogenetically analysed cases. Trisomy 21 was found in 3 cases. Trisomy of chromosome number 13 and 14 were found in 5.12% cases. Trisomy of chromosome number 3, 4, 6, 8, 11, 15, 17 and 18 were present in 2.56% cases (Fig. 21, 30, 31, 34, 35, 42). Gain of chromosome X was seen in 5.12% cases while only in one case (2.56%) gain of chromosome Y was detected. Discussion and Conclusion: Numerical chromosomal abnormality in this study was 15.38% which was different from other population described in previous studies. Trisomy 21 is most common in this study. The findings of the present study may be useful for the clinician in predicting outcome, remission, survival and treatment response in ALL.","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"71 1","pages":"283 - 287"},"PeriodicalIF":0.4,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47251062","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: In forensic anthropology, body height or stature estimation is important for identification of missing persons. Stature has a proportional relationship with different parts of the human body including cephalo-facial region. The cephalo-facial indices are different for different people. Therefore, they may help in stature reconstruction and identification of a person. The study was conducted to find out if there is any correlation between four cephalo-facial parameters and body height and to derive regression formulae in Indian and African students. Material and Methods: The present study was conducted on 170 students of a University in North India belonging to two different races, i.e., Indian (85) and African (85). Stature and four cephalo-facial dimensions, i.e., maximum head length (MHL), horizontal head circumference (HHC), morphological facial length (MFL) and bigonial diameter (BD) were measured. The data were analyzed using SPSS software version 15. Results: In both Indian and African students all the four cephalo-facial parameters, i.e., MHL, HHC, MFL, and BD showed a positive correlation with stature (P < 0.001). It was found that in Indians the strongest correlation of stature was with MHL and least correlation was with HHC. In Africans, the highest correlation was observed with MHL and lowest with BD. Discussion and Conclusion: In this study, it was found that among the cephalo-facial parameters, cephalic parameters are more reliable than facial parameters. Out of the two cephalic parameters HHC was found to be more reliable than MHL in the estimation of stature in both Indian and African students. The regression equations derived turned out to be population/race-specific and therefore, cannot be generalized for all population groups.
{"title":"Correlation of cephalo-facial parameters with body height in indian and african students of a university in North India","authors":"Sreekala M. Nair, P. Samanta, P. Kharb","doi":"10.4103/jasi.jasi_1_21","DOIUrl":"https://doi.org/10.4103/jasi.jasi_1_21","url":null,"abstract":"Introduction: In forensic anthropology, body height or stature estimation is important for identification of missing persons. Stature has a proportional relationship with different parts of the human body including cephalo-facial region. The cephalo-facial indices are different for different people. Therefore, they may help in stature reconstruction and identification of a person. The study was conducted to find out if there is any correlation between four cephalo-facial parameters and body height and to derive regression formulae in Indian and African students. Material and Methods: The present study was conducted on 170 students of a University in North India belonging to two different races, i.e., Indian (85) and African (85). Stature and four cephalo-facial dimensions, i.e., maximum head length (MHL), horizontal head circumference (HHC), morphological facial length (MFL) and bigonial diameter (BD) were measured. The data were analyzed using SPSS software version 15. Results: In both Indian and African students all the four cephalo-facial parameters, i.e., MHL, HHC, MFL, and BD showed a positive correlation with stature (P < 0.001). It was found that in Indians the strongest correlation of stature was with MHL and least correlation was with HHC. In Africans, the highest correlation was observed with MHL and lowest with BD. Discussion and Conclusion: In this study, it was found that among the cephalo-facial parameters, cephalic parameters are more reliable than facial parameters. Out of the two cephalic parameters HHC was found to be more reliable than MHL in the estimation of stature in both Indian and African students. The regression equations derived turned out to be population/race-specific and therefore, cannot be generalized for all population groups.","PeriodicalId":50010,"journal":{"name":"Journal of the Anatomical Society of India","volume":"71 1","pages":"279 - 282"},"PeriodicalIF":0.4,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48677077","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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