Rare Diseases Symptoms Automatic Extraction

Herlitz junctional epidermolysis bullosa with a novel mutation in LAMB3.

[junctional epidermolysis bullosa]

Herlitz junctional epidermolysis bullosa (H-JEB) is a rare, heritable mechanobullous disease that affects infants at birth and causes early death. This disease is primarily caused by compound heterozygous or homozygous mutations in one of three genes affecting the function of one of the three chains of the laminin-332 (formerly laminin-5) protein. Here we report a case of H-JEB with a novel heterozygous mutation in LAMB3,c.1597G>A (p.Ala533Thr). These findings attest to the molecular heterogeneity of JEB and emphasize the importance of genetic analysis to help make an accurate diagnosis, predict clinical prognosis, and identify phenotypic-genotypic relationships that may aid in prenatal diagnosis and genetic counseling for the future.

Diseases presenting "c" symptom

  • adrenomyeloneuropathy
  • alexander disease
  • cadasil
  • coats disease
  • cohen syndrome
  • dedifferentiated liposarcoma
  • epidermolysis bullosa simplex
  • erythropoietic protoporphyria
  • familial hypocalciuric hypercalcemia
  • gm1 gangliosidosis
  • homocystinuria without methylmalonic aciduria
  • junctional epidermolysis bullosa
  • kallmann syndrome
  • oligodontia
  • papillon-lefèvre syndrome
  • phenylketonuria
  • pyruvate dehydrogenase deficiency
  • von hippel-lindau disease
  • x-linked adrenoleukodystrophy

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