Literature DB >> 7648037

Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance.

E Souied1, P Amalric, M L Chauvet, C Chevallier, P Le Hoang, A Munnich, J Kaplan.   

Abstract

A familial association between juvenile macular dystrophy and congenital hypotrichosis is described in two siblings aged 25 and 23 years. We put forward arguments for locating the retinal alteration at the level of the retinal pigment epithelium and suggest that the hair disorder could be a Marie-Unna type hypotrichosis. This association is transmitted as an autosomal recessive condition.

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Year:  1995        PMID: 7648037     DOI: 10.3109/13816819509057848

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  3 in total

1.  Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy.

Authors:  Mandeep S Singh; Suzanne Broadgate; Ranjana Mathur; Richard Holt; Stephanie Halford; Robert E MacLaren
Journal:  Sci Rep       Date:  2016-05-09       Impact factor: 4.379

2.  The epidermal polarity protein Par3 is a non-cell autonomous suppressor of malignant melanoma.

Authors:  Melina Mescher; Peter Jeong; Sina K Knapp; Matthias Rübsam; Michael Saynisch; Marina Kranen; Jennifer Landsberg; Max Schlaak; Cornelia Mauch; Thomas Tüting; Carien M Niessen; Sandra Iden
Journal:  J Exp Med       Date:  2017-01-17       Impact factor: 14.307

3.  CRB1-associated retinal dystrophy presenting as self-resolving opsoclonus and posterior uveitis.

Authors:  Angela S Li; Malini Veerappan Pasricha; Kapil Mishra; Quan D Nguyen; Shannon J Beres; Edward H Wood
Journal:  Am J Ophthalmol Case Rep       Date:  2022-02-20
  3 in total

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