Phenotype #0000042450

Individual ID 00055795
Associated disease LMPHM1
Phenotype details Milroy Disease; Generalised congenital swelling when born prematurely at 32 weeks gestation. The generalised swelling rapidly resolved but he has residual lymphoedema of both feet. Family history: father has hydrocoele but no lymphoedema (has VEGFR3 mutation), cousin has congenital lymphoedema of one foot.
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset <0d
Phenotype/Onset -
Protein -
Owner name Pia Ostergaard
Database submission license No license selected
Created by Pia Ostergaard
Date created 2012-09-13 11:33:02 +02:00 (CEST)
Date last edited N/A

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