Literature DB >> 290427

A malformation complex of ectrodactyly, clefting and hypomelanosis of ito (incontinentia pigmenti achromians).

R E Stewart, S Funderburk, Y Setoguchi.   

Abstract

A case is described which, at birth, had a bizarre pattern of hypopigmentation (incontinentia pigmenti achromians), ectrodactyly involving all four extremities, and unilateral cleft lip and palate. This patient does not have the seizures or other neurological and developmental anomalies previously described as associated with hypopigmentation of Ito. This condition is also clearly different from the syndrome of ectrodactyly, ectodermal dysplasia, and clefting (EEC).

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Year:  1979        PMID: 290427

Source DB:  PubMed          Journal:  Cleft Palate J        ISSN: 0009-8701


  1 in total

1.  An unusual combination of EEC syndrome and hypomelanosis Ito due to a p63 mutation.

Authors:  Katarina Lehmann; Stefan Mundlos; Peter Meinecke
Journal:  Eur J Pediatr       Date:  2005-05-12       Impact factor: 3.183

  1 in total

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