Disease #06507 (OCNDS (Okur-Chung neurodevelopmental syndrome), OMIM:617062)

Official abbreviation OCNDS
Name Okur-Chung neurodevelopmental syndrome
OMIM ID 617062
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CSNK2A1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00464073 patient PubMed: Akahira-Azuma 2018 2-generation family, 1 affected, unaffected non carrier parents M - Japan - - - - - OCNDS see paper; ..., 40w+6 birth, birth weight 2740 g, length 47.5 cm, OFC 33.0 cm; delayed developmental milestones, 4m-head control, 12m-sit; 1y4m-hypotonia, decreased muscle bulk, non-verbal, MRI brain reduced anterior pituitary gland/delayed myelination; 2y-10m-distinct facial features, synophrys, hypertrichosis, down-slanting palpebral fissures, bulbous nose; severe growth retardation, relative macrocephaly, friendly, hyperactive behavior, intellectual disability - CSNK2A1 1 1 Johan den Dunnen
00464617 321367 - - M no Germany - - - - - OCNDS EEG abnormality, Neurodevelopmental delay, Poor or absent speech CSNK2A1 CSNK2A1 1 1 Andreas Laner
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