All individuals with variants in gene CCT5

5 entries on 1 page. Showing entries 1 - 5.
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00078903 - PubMed: Bouhouche 2006 4-generation family, 4 affected brothers M yes Morocco - - - - - ? neuropathy, hereditary sensory, with spastic paraplegia; spastic paraplegia, progressive sensory loss, mutilating acropathy involving both upper/lower limbs; MRI severe atrophy spinal cord predominantly posterior tract 1 133 Johan den Dunnen
00078904 - PubMed: Bouhouche 2006 4-generation family, 5 unaffected carriers - yes Morocco - - - - - Healthy/Control - 1 134 Johan den Dunnen
00108467 28722276-FamPatIII3 PubMed: Hendee 2017, Journal: Hendee 2017 3-generation family, 10 affecteds (6F, 4M), PatIII3 M - United States white - - - - ? Congenital glaucoma Axenfeld-Rieger anomaly myopia sensorineural hearing loss congenital hypothyroidism arterial tortuosity microcephaly delayed eruption of permanent teeth femoral retroversion 1 1 Elena Semina
00207795 - - - F - Germany - - - - - - HP:0002527 (Falls); HP:0001288 (Gait disturbance); HP:0000762 (Decreased nerve conduction velocity); HP:0009130 (Hand muscle atrophy); HP:0003394 (Muscle cramps); HP:0001436 (Abnormality of the foot musculature); HP:0007010 (Poor fine motor coordination) 1 1 Andreas Laner
00293685 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 246 Mohammed Faruq
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