Phenotype #0000272166

Individual ID	00376973
Associated disease	CDG
Diagnosis/Initial	congenital glycosylation disorder
Diagnosis/Definite	-
Phenotype details	birth full term, weight 3050g, length 45cm, OFC 34cm; length 154cm (-1.2SD), OFC 54cm (-0.5SD), weight 67kg (+0.6SD); moderate intellectual disability; developmental delay; speech delay; no seizures; no hypotonia; anxiety; narrow palpebral fissures; no epicanthal folds; no increased nasal height; no bulbous tip; low columella; no smooth philtrum; no short philtrum; thin upper lip; no retrognatia; no eye abnormalities; no ear abnormalities; normal extremities; no genital abnormalities
Inheritance	Familial, autosomal recessive
Age/Examination	22y (22 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Johan den Dunnen
Date created	2021-06-28 16:11:27 +02:00 (CEST)
Date last edited	N/A

Global Variome shared LOVD