Literature DB >> 911172

Chondrodysplasia punctata. Conradi-Hünermann syndrome.

D V Edidin, N B Esterly, A K Bamzai, D F Fretzin.   

Abstract

A 10-day-old girl was examined because of a peculiar, patterned hyperkeratosis that was noted at birth. The lesions were distributed over the trunk and limbs and consisted of whorls and streaks of thick, yellow, adherent scales. The salient histologic feature was marked hyperkeratosis with deep invagination of the dilated pilosebaceous ostia nearly to the level of the hair bulb. Additional physical abnormalities included patchy alopecia, bilateral zonular cataracts, a depressed nasal bridge, small stature, and multiple skeletal deformities. Roentgenograms demonstrated widespread stippled epiphyses characteristic of Conradi-Hünermann syndrome.

Entities:  

Mesh:

Year:  1977        PMID: 911172

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  5 in total

1.  Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography.

Authors:  R P Clark; M R Goff; K D MacDermot
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

Review 2.  Lyonization and the lines of Blaschko.

Authors:  R Happle
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  X-linked dominant chondrodysplasia punctata. Review of literature and report of a case.

Authors:  R Happle
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

4.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Ichthyosis and osteopetrosis.

Authors:  P M Dowd; D D Munro
Journal:  J R Soc Med       Date:  1983-05       Impact factor: 18.000

  5 in total

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