Overgrowth syndrome
MONDO:0019716A group of syndromes caused by genetic birth defects that may lead to the development of malignancies. It is characterized by a large body size or large body parts at birth, or excessive body growth early in childhood. Representative examples include neurofibromatosis, Beckwith-Wiedemann syndrome, and Sturge-Weber syndrome.
45 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
PIK3CA-related overgrowth spectrum
(15)
Simpson-Golabi-Behmel syndrome
(11)
Angioosteohypertrophic syndrome
(6)
Beckwith-Wiedemann syndrome
(5)
CLOVES syndrome
(5)
Hemifacial hypertrophy
(3)
Megalencephaly-capillary malformation-polymicrogyria syndrome
(3)
Maffucci syndrome
(2)
Proteus syndrome
(2)
Bannayan-Riley-Ruvalcaba syndrome
(1)
Hyperinsulinemic hypoglycemia, familial, 2
(1)
Hyperinsulinism-hyperammonemia syndrome
(1)
11p15.4 microduplication syndrome
(0)
15q overgrowth syndrome
(0)
4p16.3 microduplication syndrome
(0)
AKT3-related overgrowth spectrum
(0)
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
(0)
Autosomal dominant hyperinsulinism due to SUR1 deficiency
(0)
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
(0)
Autosomal recessive hyperinsulinism due to SUR1 deficiency
(0)