Literature DB >> 23778732

Johanson-blizzard syndrome.

Koumudi Godbole1, Sukalo Maja, Hiremath Leena, Zenker Martin.   

Abstract

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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Year:  2013        PMID: 23778732

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  3 in total

1.  Johanson-Blizzard syndrome: hepatic and hematological features with novel genotype.

Authors:  Ankur Singh; Neha Chaudhary; Dhulika Dhingra; Maja Sukalo; Martin Zenker; Seema Kapoor
Journal:  Indian J Gastroenterol       Date:  2013-09-20

2.  A Case with Complete Pancreatic Aplasia Suggestive of Johanson-Blizzard Syndrome.

Authors:  Seyed Ali Jafari; Roozbeh Moghaddar; Mohammad Bahadoram; Hamid Reza Kianifar; Mehran Beiraghi Tosi
Journal:  J Clin Diagn Res       Date:  2016-08-01

3.  Congenital absence of the nasal septum in a Nigerian newborn with multiple congenital anomalies.

Authors:  Isa Abdulkadir; Sani Musa; Fatima Lami Abdullahi; Laila Hassan
Journal:  BMJ Case Rep       Date:  2020-09-07
  3 in total

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