Phenotypes for disease #05519 (AOA (ataxia-oculomotor apraxia (AOA)))

14 entries on 1 page. Showing entries 1 - 14.
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0000154696 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206904
0000154697 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206905
0000154698 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206906
0000154699 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206907
0000154700 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206908
0000154701 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206909
0000154702 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206910
0000154703 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206911
0000154704 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206912
0000154705 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206913
0000154706 ataxia-oculomotor apraxia AOA-4 see paper; … Familial, autosomal recessive - - - - - Johan den Dunnen 00206914
0000290701 Ataxia Ataxia with ocular motor apraxia type 1 Developmental history: The patient is a product of normal pregnancy and delivery (dizygotic twin but the other is twin is completely normal). Normal developmental milestones Family history: History of consanguineous marriage (cousins) The patient has one brother with similar illness started at the age of 8. His brother developed incoordination during walking and frequent fall on the ground. He had nystagmus (end-gaze). History of present illness: The patient developed an insidious illness in the form of progressive incoordination. He dysarthria (staccato speech), nystagmus and change in the foot shape in the form of flat foot. No history suggestive of peripheral nerve affection, no sensory system affection, no sphincteric disturbance, no cognitive deterioration. No cranial nerve involvement. Normal power. Neurological examination: Limb girdle ataxia Nystagmus Staccato speech Normal sensation Flat foot Wide base staggering gaze Normal planter response Familial, autosomal recessive 17y 24y 08y Ataxia - Sherifa Ahmed Hamed 00397578
0000296712 - AOA2 32-y male with progressive ataxia, ocular apraxia, peripheral neuropathy and bilateral Babinski sign Familial, autosomal recessive 27y - 16y - - Sherifa Ahmed Hamed 00404123
0000296713 - AOA1 18-y male with progressive ataxia and abnormal ocular eye movement. Familial, autosomal recessive 15y - 07y - - Sherifa Ahmed Hamed 00404124
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