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Indian Pediatr ; 2013 May; 50(5): 510-512
Artigo em Inglês | IMSEAR | ID: sea-169814

RESUMO

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.

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