Congenital primary lymphedema of Gordon

Orpha code: 569821OMIM code:

Definicja

A rare primary lymphedema characterized by bilateral, painless lower limb swelling present at birth. Prominent veins around the ankles and on the dorsa of the feet, dysplastic and upslanting toenails due to edema of the nailbed, and subtle dysmorphic facial features (such as high forehead, hypertelorism, depressed nasal bridge, mild bilateral ear dysplasia, and short neck) have also been described. The degree of lymphatic impairment is milder than in the otherwise clinically similar Milroy disease, as evidenced by slightly less severe lymphedema and significantly more uptake of tracers on lymphoscintigraphy.

Disease data
Klasyfikacja

Disease

Synonimy
VEGFC-related congenital primary lymphedema
VEGFC-related congenital primary lymphedema
Kod ORPHA
569821
Kod OMIM
-
Kod ICD10
-
Kod ICD11
-

No additional description.

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