Phenotype #0000042426

Individual ID	00055771
Associated disease	LMPHM1
Phenotype details	Milroy Disease, half-sister, mutation positive. First seen at 11yr of age: bilateral lymphoedema of lower limbs and feet. Varicose veins. Venous ultrasound imaging revealed insufficiency of sapheno-femoral junction and greater saphenous vein.; First seen at 2 yr of age: unilateral lymphoedema of left lower limb and foot.
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	2y
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Pia Ostergaard
Database submission license	No license selected
Created by	Pia Ostergaard
Date created	2012-07-13 15:27:53 +02:00 (CEST)
Date last edited	2012-07-13 16:30:22 +02:00 (CEST)

Global Variome shared LOVD