Phenotypes for disease #05779 (COFS (cerebrooculofacioskeletal syndrome (COFS)))

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0000231957 severe cerebro-oculo-facial-skeletal syndrome COFS4 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 Familial, autosomal recessive 00y14m 00y00m01d - - Johan den Dunnen 00306116
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