Angiokeratoma corporis diffusum. Some clinical aspects.
Open Access
- 1 February 1968
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 43 (227) , 73-79
- https://doi.org/10.1136/adc.43.227.73
Abstract
A large family with the X-linked disease angiokeratoma corporis diffusum is reported. Attention is drawn to the variation in symptoms and signs and to the diagnostic difficulties, particularly in children.This publication has 19 references indexed in Scilit:
- Genetic aspects of angiokeratoma corporis diffusumAnnals of Human Genetics, 1966
- Fabry's disease—glycolipid lipidosis: Histochemical and electron microscopic studies of two casesThe American Journal of Medicine, 1966
- Angiokeratoma Corporis Diffusum (FABRY)Journal of Investigative Dermatology, 1965
- The Ocular Manifestations of Hereditary Dystopic LipidosisArchives of Ophthalmology (1950), 1963
- Angiokeratoma Corporis Diffusum Universale (Fabry's Disease) in Two BrothersNew England Journal of Medicine, 1961
- Angiokeratoma Corporis Diffusum—A Case ReportPublished by American Medical Association (AMA) ,1961
- ANGIOKERATOMA CORPORIS DIFFUSUM.British Journal of Dermatology, 1955
- Angiomatosis bzw. Angiokeratosis universalis (eine sehr seltene Haut- und Gefäßerkrankung)Deutsche Medizinische Wochenschrift (1946), 1925
- Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis (Purpura papulosa haemorrhagica Hebrae)Archives of Dermatological Research, 1898
- A CASE OF “ANGEIO-KERATOMA.”British Journal of Dermatology, 1898