Disease #01761 (DKCB1 (dyskeratosis congenita, autosomal recessive, type 1 (DKCB-1)), OMIM:224230)

Official abbreviation DKCB1
Name dyskeratosis congenita, autosomal recessive, type 1 (DKCB-1)
OMIM ID 224230
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NOP10
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00052951 - PubMed: Walne 2007, Journal: Walne 2007 2-generation family, 3 affecteds (2F, M), unaffected heterozygous carrier parents/sibs - yes Saudi Arabia Arab - - - - DKCB1 ages diagnosis II2 16y, II3 20y, II5 15y; all reticular skin pigmentation over neck and upper extremities, thickening skin palms/soles; dystrophic changes nails, abnormal dentition (II3, II5 less severe); II2 hypocellular bone marrow with peripheral pancytopenia was only observed; no leukoplakia NOP10 NOP10 1 3 Johan den Dunnen
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