Literature DB >> 3794888

Rapp-Hodgkin ectodermal dysplasia.

H W Schroeder, V P Sybert.   

Abstract

Rapp-Hodgkin ectodermal dysplasia is an autosomal dominant condition characterized by distinctive craniofacies, cleft lip or palate, dental hypoplasia with caries, dystrophic nails, and decreased to absent sweat glands and hair follicles. We report the third family to be described, and distinguish the condition from similar syndromes.

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Year:  1987        PMID: 3794888     DOI: 10.1016/s0022-3476(87)80291-3

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  2 in total

1.  Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia.

Authors:  J Goodship; S Malcolm; A Clarke; M E Pembrey
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

2.  Ectodermal Dysplasia Showing the Clinical Overlap between Hay Wells Syndrome and Bowen Armstrong Syndrome.

Authors:  Andreea Liana Rachisan; Simona Cainap; Mariana Andreica; Nicolae Miu
Journal:  Iran J Pediatr       Date:  2011-03       Impact factor: 0.364

  2 in total

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