Disease #06247 (GLOW (GLOW syndrome, somatic mosaic), OMIM:618272)

Official abbreviation GLOW
Name GLOW syndrome, somatic mosaic
OMIM ID 618272
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DICER1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00399726 patient PubMed: Ponten 2022 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Sweden - - - - - GLOW see paper; ...; normal length, normal weight, pronounced macrocephaly (>99th), dysmorphic features, broad furrowed forehead, wide mouth, tooth anomalies, doughy, soft skin, multiple nevi, intellectual disability, autism, behavioural problems, surgical treatment due to left-convex thoracic scoliosis DICER1 DICER1 2 1 Johan den Dunnen
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