Disease #05779 (COFS (cerebrooculofacioskeletal syndrome (COFS)))

Official abbreviation COFS
Name cerebrooculofacioskeletal syndrome (COFS)
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ERCC1
Associated tissues -
Disease features -
Remarks -
Date created 2020-07-08 13:41:42 +02:00 (CEST)
Date last edited N/A


Individuals

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00306116 Pat165TOR PubMed: Jaspers 2007 2-generation family, 1 affected, unaffected heterozygous carrier parents - no Italy white 00y14m - - - COFS pregnancy intrauterine growth retardation; birth 37w, weight, length, and OFC <3rd percentile; microcephaly, premature closure of fontanels, bilateral microphthalmia, blepharophimosis, high nasal bridge, short filtrum, micrognathia, low-set ears, posterior-rotated ears, arthrogryposis with rocker-bottom feet , flexion contractures hands, bilateral congenital hip dislocation; X-rays no spine abnormalities; NMR simplified gyral pattern, cerebellar hypoplasia; mild hypoplasia kidneys with normal structure and function; echography no congenital heart defects; no genital abnormalities, no retinopathy; failure to thrive, tube feeding, did not pass any developmental milestone; 14m-deceased of respiratory failure due to bilateral pneumonia, weight 4.5 kg, height 56 cm, OFC 38 cm ERCC1 ERCC1 2 1 Johan den Dunnen
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