[Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant].
Identifieur interne : 00D918 ( Main/Exploration ); précédent : 00D917; suivant : 00D919[Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant].
Auteurs : N. Kubryk ; M. RogerSource :
- Annales de pediatrie [ 0066-2097 ] ; 1990.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphoedème.
- génétique : Lymphoedème.
- Diagnostic différentiel, Humains, Lymphoedème, Mâle, Nourrisson, Pedigree.
English descriptors
- KwdEn :
- MESH :
- congenital : Lymphedema.
- diagnosis : Lymphedema.
- genetics : Lymphedema.
- Diagnosis, Differential, Humans, Infant, Male, Pedigree.
Abstract
A case of Milroy disease is reported. This very infrequent condition is a familial disease characterized by the presence of lymphedema of the lower limbs. In our patient's family, we identified 12 affected members belonging to four generations.
PubMed: 2256646
Affiliations:
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Le document en format XML
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