Phenotypes for disease #04086 (SSMCF (stature, short, with microcephaly and distinctive facies), OMIM:615789)

2 entries on 1 page. Showing entries 1 - 2.
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Phenotype details     

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Individual ID     
0000078884 microcephalic primordial dwarfism; birth 40w, weight 2700g (-1.8), OFC 0.4th centile; 7y2m, weight 14.24kg (-4.6), length 105.6cm (-3.3), OFC 42.4 cm (-6.5). Mild to moderate developmental delay (HP:0001263), Delayed bone age (HP:0002750), 5th finger clinodactyly (HP:0004209) & brachydactyly (HP:0009237) No active movement in 1st Interphalangeal Joints (IPJ), Tremor (HP:0001337), (1.6Mb Xp22.31 dup on arrayCGH), blepharophymosis, broad nasal bridge (HP:0000431), cupped ears (HP:0000378), tall forehead(HP:0000348), short tapering fingers (HP:0001182) - - Familial, autosomal recessive 07y02m - 00y00m00d - - Lynn Boekhoudt 00100659
0000289344 Abnormal hair morphology, Cutis marmorata, Failure to thrive, Short stature, Microcephaly, Ulnar deviation of the hand or of fingers of the hand - - Familial, autosomal recessive - 01y - - - Andreas Laner 00396178
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