17q12 微缺失综合征

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2024-11-07 DOI:10.1136/bcr-2024-262697
Viswanadhula S L V Bhargav, Mahesh Venkatachari, Thirunavukkarasu Arun Babu
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引用次数: 0

摘要

一名女婴出现全身多处水疱,随后脱皮,持续 5 天,前驱症状为发烧和咳嗽。患儿面容畸形,发育迟缓。腹部超声波检查显示,双肾多发小囊肿,回声增强,皮质髓质分化消失。全外显子组测序显示,17号染色体长臂上有1.4 mb的缺失,其中还涉及HNF1B基因。糖尿病检查结果显示,患者的 HbA1c 为 5.9%,空腹血糖水平正常,提示可能患有糖尿病前期。该患儿的肾功能异常,肾小球滤过率(GFR)估计为 22 mL/min/1.73 m2,可能患有葡萄球菌皮肤烫伤综合征(SSSS)。本病例描述了 17q12 缺失综合征的非典型表现,即早发性慢性肾病、糖尿病前期和 SSSS。
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17q12 microdeletion syndrome.

An infant girl presented with multiple blisters followed by peeling of the skin over the entire body for 5 days with a prodrome of fever and cough. The child had dysmorphic facies, growth faltering and developmental delay. The ultrasonogram of the abdomen showed multiple small cysts in both kidneys with increased echogenicity and loss of corticomedullary differentiation. The whole exome sequencing revealed a 1.4 mb deletion on the long arm of chromosome 17, which also involves HNF1B gene. Diabetes workup showed an HbA1c of 5.9% with normal fasting glucose levels suggestive of a possible pre-diabetes. The renal functions were deranged with an estimated GFR of 22 mL/min/1.73 m2 Keeping a possibility of staphylococcal scalded skin syndrome (SSSS), the child was treated successfully with appropriate antibiotics. This case depicts atypical presentation of 17q12 deletion syndrome with a very early onset chronic kidney disease, pre-diabetes and SSSS.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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