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Prenatal diagnosis of anhidrotic ectodermal dysplasia
Author(s) -
Arnold M.L.,
Rauskolb R.,
AntonLamprecht I.,
Schinzel A.,
Schmid W.
Publication year - 1984
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1970040202
Subject(s) - ectodermal dysplasia , vellus hair , fetoscopy , fetus , medicine , prenatal diagnosis , dysplasia , proband , pregnancy , pathology , skin biopsy , dermatology , biopsy , anatomy , biology , scalp , biochemistry , gene , mutation , genetics
This paper reports on successful prenatal diagnosis of X‐linked anhidrotic ectodermal dysplasia (AED) by means of light and electron microscopy on fetal skin biopsies obtained under fetoscopy. In the present family two brothers of the proband were severely affected with the full symptomatology of AED, the pregnant female and her mother revealed minor symptoms with patches of skin lacking vellus hair. Control of lesional skin of the affected family members by electron microscopy revealed no ultrastructural abnormalities. However, all biopsies lacked skin appendages including hair follicles, sebaceous glands, and sweat glands. The lack of pilosebaceous follicles can be used as a diagnostic criterion since these structures are fully developed in normal fetuses of 20 weeks whereas the development of sweat glands does not start before week 20 to 24 of fetal life. Skin biopsies were taken from various regions of the fetus at risk via fetoscopy in week 20 and processed for light and electron microscopy. All samples revealed complete absence of all skin appendages in contrast to a total of 61 non‐AED fetuses. Thus positive prenatal diagnosis of AED was made and the pregnancy was terminated. Control investigations after abortion confirmed the diagnosis.