Dawid Gruszczyński, Kacper Nijakowski, A. Wolska-Bułach, K. Lacka
{"title":"性染色体异常患者的骨骼和牙齿异常:一项系统的基于病例的回顾","authors":"Dawid Gruszczyński, Kacper Nijakowski, A. Wolska-Bułach, K. Lacka","doi":"10.5114/polp.2022.114705","DOIUrl":null,"url":null,"abstract":"Sex chromosome aneuploidies (SCAs) are common chromosomal disorders characterised by an atypical number of sex chromosomes. Turner syndrome (TS), Klinefelter syndrome (KS), and Jacobs syndrome (JS) are associated with a wide spectrum of skeletal manifestations, including craniofacial and limb anomalies. This systematic review aimed to analyse the incidence of skeletal abnormalities in selected SCAs based on case reports. In this review, 55 articles were included from the MEDLINE/PubMed and Google Scholar databases, according to PRISMA guidelines. High-arched palate, skeletal class II, and cubitus valgus were most frequently demonstrated among TS patients. Patients with KS and JS most often presented micrognathia, hypertelorism, and flat nasal bridge in the craniofacial region. In contrast, radioulnar synostosis, clinodactyly, and pes planus could be observed in the limbs of KS patients. The presence of dysmorphic facial features and limb malformations may indicate SCAs, which are underdiagnosed in the general population due to a variety of phenotypes.","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Skeletal and dental abnormalities in patients with sex chromosome aberrations: a systematic case-based review\",\"authors\":\"Dawid Gruszczyński, Kacper Nijakowski, A. Wolska-Bułach, K. Lacka\",\"doi\":\"10.5114/polp.2022.114705\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sex chromosome aneuploidies (SCAs) are common chromosomal disorders characterised by an atypical number of sex chromosomes. Turner syndrome (TS), Klinefelter syndrome (KS), and Jacobs syndrome (JS) are associated with a wide spectrum of skeletal manifestations, including craniofacial and limb anomalies. This systematic review aimed to analyse the incidence of skeletal abnormalities in selected SCAs based on case reports. In this review, 55 articles were included from the MEDLINE/PubMed and Google Scholar databases, according to PRISMA guidelines. High-arched palate, skeletal class II, and cubitus valgus were most frequently demonstrated among TS patients. Patients with KS and JS most often presented micrognathia, hypertelorism, and flat nasal bridge in the craniofacial region. In contrast, radioulnar synostosis, clinodactyly, and pes planus could be observed in the limbs of KS patients. The presence of dysmorphic facial features and limb malformations may indicate SCAs, which are underdiagnosed in the general population due to a variety of phenotypes.\",\"PeriodicalId\":39653,\"journal\":{\"name\":\"Pediatria Polska\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pediatria Polska\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5114/polp.2022.114705\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatria Polska","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5114/polp.2022.114705","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Skeletal and dental abnormalities in patients with sex chromosome aberrations: a systematic case-based review
Sex chromosome aneuploidies (SCAs) are common chromosomal disorders characterised by an atypical number of sex chromosomes. Turner syndrome (TS), Klinefelter syndrome (KS), and Jacobs syndrome (JS) are associated with a wide spectrum of skeletal manifestations, including craniofacial and limb anomalies. This systematic review aimed to analyse the incidence of skeletal abnormalities in selected SCAs based on case reports. In this review, 55 articles were included from the MEDLINE/PubMed and Google Scholar databases, according to PRISMA guidelines. High-arched palate, skeletal class II, and cubitus valgus were most frequently demonstrated among TS patients. Patients with KS and JS most often presented micrognathia, hypertelorism, and flat nasal bridge in the craniofacial region. In contrast, radioulnar synostosis, clinodactyly, and pes planus could be observed in the limbs of KS patients. The presence of dysmorphic facial features and limb malformations may indicate SCAs, which are underdiagnosed in the general population due to a variety of phenotypes.
Pediatria PolskaMedicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
19
期刊介绍:
Pediatria Polska - rzetelna wiedza i tradycja. Organ Polskiego Towarzystwa Pediatrycznego. Ukazuje się od 1921 roku, poprzednio w latach 1908-1920 jako Przegląd Pedyatryczny. Drugie obok Otolaryngologii Polskiej najstarsze czasopismo medyczne ukazujące się na polskim rynku. Czasopismo zamieszcza doświadczalne i kliniczne prace oryginalne oraz opisy rzadko występujących i trudnych diagnostycznie przypadków klinicznych. W Pediatrii Polskiej publikowane są także obszerne omówienia poglądowe problemów pediatrycznych oparte na najnowszym piśmiennictwie światowym.