Your browser doesn't support javascript.
loading
Delayed Presentation of Respiratory Symptoms and Prolonged Survival in Homozygous a3 Integrin Deficiency
Indian Pediatr ; 2020 Mar; 57(3): 268-269
Article | IMSEAR | ID: sea-199514
ABSTRACT
Interstitial lung disease with nephrotic syndrome and junctionalepidermolysis bullosa is caused by biallelic mutations in theintegrin gene ITGA3 and is associated with death in infancy. Wedescribe a variant of this syndrome with delayed presentation ofsymptoms and prolonged survival.

Full text: Available Index: IMSEAR (South-East Asia) Type of study: Diagnostic study Journal: Indian Pediatr Year: 2020 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: IMSEAR (South-East Asia) Type of study: Diagnostic study Journal: Indian Pediatr Year: 2020 Type: Article