Disease #05853 (CHANDS (CHAND syndrome), OMIM:214350)

Official abbreviation CHANDS
Name CHAND syndrome
OMIM ID 214350
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene RIPK4
Associated tissues -
Disease features -
Remarks -
Date created 2020-10-15 08:50:59 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00462249 Pat2 PubMed: Busa 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Tunisia - - - - - CHANDS see paper; ..., birth-38w, weight 2820g (20th centile), length 47cm (13th centile), OFC 34cm (41th centile), ankyloblepharon (required early surgery; ECG normal, ultrasound brain normal, normal retina; abdominal ultrasound unilateral ureteral dilatation; 1m-nail dysplasia, dry skin, bifid tongue, multiple oral frenula; 3y-deciduous teeth normal, hair curly, hair wooly, hair sparse; normal growth parameters; normal motor development, 13m-walk; slight speech delay,attended regular school RIPK4, TP63 RIPK4 1 1 Johan den Dunnen
00462250 family 5-generation family, 3 affected (2f, M), unaffected heterozygous carrier parents/relatives PubMed: Gollasch 2015 F;M yes Kuwait - - - - - CHANDS see paper; ..., ankyloblepharon, sparse hair, curly hair, hypoplastic nails RIPK4 RIPK4 1 3 Johan den Dunnen
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