Department of Genetic Medicine, Deenanath Mangeshkar Hospital and Research Center, Erandawane, Pune, India.
Indian Pediatr. 2013 May 8;50(5):510-2.
We present clinical features and genetic diagnosis in an Indian infant diagnosed with Johanson- Blizzard syndrome. This is a rare, autosomal recessive genetic condition with multi-system involvement and a characteristic facies. Molecular genetic testing is important to confirm the clinical diagnosis and offer prenatal diagnosis in future pregnancies.
我们介绍了一位被诊断为 Johanson-Blizzard 综合征的印度婴儿的临床特征和基因诊断。这是一种罕见的常染色体隐性遗传疾病,多系统受累,具有特征性面容。分子遗传学检测对于确认临床诊断和为未来妊娠提供产前诊断非常重要。