Phenotypes for disease #05853 (CHANDS (CHAND syndrome), OMIM:214350)

2 entries on 1 page. Showing entries 1 - 2.
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Individual ID     
0000349749 CHAND syndrome CHAND see paper; ..., birth-38w, weight 2820g (20th centile), length 47cm (13th centile), OFC 34cm (41th centile), ankyloblepharon (required early surgery; ECG normal, ultrasound brain normal, normal retina; abdominal ultrasound unilateral ureteral dilatation; 1m-nail dysplasia, dry skin, bifid tongue, multiple oral frenula; 3y-deciduous teeth normal, hair curly, hair wooly, hair sparse; normal growth parameters; normal motor development, 13m-walk; slight speech delay,attended regular school Familial, autosomal recessive 03y - - - Johan den Dunnen 00462249
0000349750 CHAND syndrome CHAND see paper; ..., ankyloblepharon, sparse hair, curly hair, hypoplastic nails Familial, autosomal recessive - - - - Johan den Dunnen 00462250
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