Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome

Disease Export to PDF
Name:
Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
Description:
A life-threatening multiorgan disorder which develops in the first months of life, presenting with respiratory distress and proteinuria in the nephrotic range, and leading to severe interstitial lung disease and renal failure. Some patients additionally display cutaneous alterations, ranging from blistering and skin erosions to an epidermolysis bullosa-like phenotype, with toe nail dystrophy and sparse hair.
ORPHAcode:
306504
Synonyms:
ILNEB syndrome
JEB with interstitial lung disease and nephrotic syndrome
Junctional epidermolysis bullosa with interstitial lung disease and nephrotic syndrome
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14