Disease #04273 (ICF (immunodeficiency-centromeric instability-facial anomalies syndrome (ICF)))

Official abbreviation ICF
Name immunodeficiency-centromeric instability-facial anomalies syndrome (ICF)
OMIM ID -
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 4 genes CDCA7, DNMT3B, HELLS, ZBTB24
Associated tissues -
Disease features -
Remarks -
Date created 2015-05-18 08:56:14 +02:00 (CEST)
Date last edited N/A


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00038699 - PubMed: Thijssen 2015 female from 2-generation family E (2 affected sibs), unaffected heterozygous carrier parents F no United Kingdom (Great Britain) English >15y - - stem cell transplantation ICF facial anomalies (HP:0001999), gastrointestinal problems (chronic diarrhea HP:0002028), infections (pneumonia, pneumocystis); IgG <<0.33 g/l, IgA <0.07g/l, IgM 0.10g/l HELLS HELLS 2 1 Peter Thijssen
00038700 - PubMed: Thijssen 2015 male from 2-generation family E (2 affected sibs), unaffected heterozygous carrier parents M no United Kingdom (Great Britain) English >08y - - stem cell transplantation ICF facial anomalies (HP:0001999), no gastrointestinal problems; IgG 8.05 g/l (maternal), IgA <0.3 g/l, IgM <0.22 g/l HELLS HELLS 2 1 Peter Thijssen
00038701 - PubMed: Thijssen 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents F ? Japan Japanese 01y03m - - - ICF facial anomalies (HP:0001999), no gastrointestinal problems, infections (pneumonia, pneumocystis); IgG 0.23 g/l, IgA 0.06g/l, IgM 0.05 g/l; cytogenetic abnormalities include stretching, associations, rosettes, branching, micronuclei, decondensation HELLS HELLS 1 1 Peter Thijssen
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