All individuals with variants in gene FAM111B

2 entries on 1 page. Showing entries 1 - 2.
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00029685 - PubMed: Mercier, Küry, Shaboodien, Houniet 2013, Journal: Mercier, Küry, Shaboodien, Houniet et al (2013) 2-generation family, 1 affected, 3 unaffected non-carriers M no France white - - - - POIKTMP Photodistributed poikiloderma, eczematous lesions of the hands and feet, alopecia, heat intolerance, hypohidrosis. Progressive muscle weakness and tendon contractures of both feet. Myogenic pattern of the lower limbs (by EMG), diffuse fatty infiltration of skeletal muscle (by MRI). 1 1 Sébastien Küry
00320137 - - - M - - - - - - - ? Sparse and thin eyebrow (HP:0000535); Sparse eyelashes (HP:0000653); Muscle weakness (HP:0001324); Sparse scalp hair (HP:0002209); Hypocalcemia (HP:0002901); Hypomagnesemia (HP:0002917); Severe photosensitivity (HP:0007537) 1 1 IMGAG
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