Familial acrogeria (Gottron)
- 1 August 1980
- journal article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 103 (2) , 213-223
- https://doi.org/10.1111/j.1365-2133.1980.tb06595.x
Abstract
A mother and her oldest son suffering from acrogeria are described; in the mother the disease was complicated by elastosis perforans serpiginosa. Microscopic and ultramicroscopic details are given.Keywords
This publication has 11 references indexed in Scilit:
- Inheritance of Ehlers-Danlos type IV syndrome.Journal of Medical Genetics, 1977
- AcrogeriaDermatology, 1977
- The premature ageing syndromes.British Journal of Dermatology, 1974
- L’acrogéria est-elle une maladie du fibroblaste?Dermatology, 1974
- Die Akrogerie (Gottron)Deutsche Medizinische Wochenschrift (1946), 1970
- Variants of the Ehlers-Danlos syndrome. Clinical, biochemical, haematological, and chromosomal features of 100 patients.Annals of the Rheumatic Diseases, 1969
- Heterogeneity of the Ehlers-Danlos syndrome: description of three clinical types and a hypothesis to explain the basic defect(s).BMJ, 1967
- Die Akrogerie (Gottron)Archives of Dermatological Research, 1960
- OXFORD DERMATOLOGICAL GROUPBritish Journal of Dermatology, 1957
- Familiäre AkrogerieArchives of Dermatological Research, 1940