All individuals with variants in gene KY

6 entries on 1 page. Showing entries 1 - 6.
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00063263 - - - F yes - - - - - - MYOP - 1 1 Carola Hedberg-Oldfors
00265880 03443 - - F yes Pakistan - - - - - neuropathy, peripheral - 1 1 Beenish Arif
00295568 - - - F - - - - - - - ? Weakness due to upper motor neuron dysfunction (HP:0010549); Abnormality of muscle morphology (HP:0011805); Tetraparesis (HP:0002273); Myopathy (HP:0003198) 1 1 Andreas Laner
00473062 Fam12695Pat176 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - LGMD Age at diagnosis: 23y, Hx. of delayed motor milestone; Proximal & distal muscle weakness; Decreased muscle force; Lumbar lordosis; Muscle wasting at shoulder girdle; Waddling gait; Achilles tendon contractures; Wheelchair bound; Hx of spinal tumor, cellular schwannoma & hypothyroidism; Lower limb MRI: fatty atrophy; Echocardiography: mild MVP, PI & TR, trivial MR, AR; Elevated CPK; EMG-NCV: chronic myopathic process; Muscle biopsies: suggestive of SMA, type 3 & LGMD. 1 1 Johan den Dunnen
00473312 Fam203072Pat551 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history M yes Iran - - - - - NMD Muscle weakness, progressive; EMG-NCV: compatible with myopathic disorder, probably limb girdle muscular dystrophy; Positive FHx of similar disorder 1 1 Johan den Dunnen
00473509 Fam8606961Pat878 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history M yes Iran - - - - - MYOP sporadic case, started 12y with tip toe walking,climbing difficulty,dysarthria, dysphagia, gait abnormality, severe myopathy reported in EMG,slightly atrophic changes with fiber types uniformity reported in muscle biopsy, slightly elavated LDH abd CPK 1 1 Johan den Dunnen
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