Regional choroidal atrophy and alopecia. A new syndrome

Two siblings with total regional choroidal atrophy and other manifestations of ectodermal dysplasia are presented. The mode of inheritance is uncertain, but mild macular disease in the father may represent heterozygote manifestation of a recessive condition.

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Bibliographic Details
Published inActa ophthalmologica Vol. 66; no. 3; p. 272
Main Authors Moloney, J B, Blake, J, Denham, B, Mooney, D
Format Journal Article
LanguageEnglish
Published Denmark 01.06.1988
Subjects
Adult
Alopecia - genetics
Alopecia - pathology
Child
Child, Preschool
Electrooculography
Female
Fluorescein Angiography
Gyrate Atrophy - genetics
Gyrate Atrophy - pathology
Gyrate Atrophy - physiopathology
Humans
Macula Lutea - pathology
Macula Lutea - physiopathology
Male
Scalp - pathology
Visual Acuity
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Summary:Two siblings with total regional choroidal atrophy and other manifestations of ectodermal dysplasia are presented. The mode of inheritance is uncertain, but mild macular disease in the father may represent heterozygote manifestation of a recessive condition.
ISSN:0001-639X
DOI:10.1111/j.1755-3768.1988.tb04596.x