All individuals with variants in gene UCP1

3 entries on 1 page. Showing entries 1 - 3.
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00019912 - PubMed: Gilissen 2014 - ? ? - - - - - - ID severe ID, severe epilepsy, Rett-like phenotype, motor handicap, severe feeding difficulties, progressive scoliosis 1 1 Marianne Vos (LOVD-team)
00050566 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, high forehead, dental crowding, hypopigmented skin patches 1 1 Johan den Dunnen
00327463 M69 II-1 Doucette 2021, Submitted Affected sister in a 4 member family. Brother is reportedly affected however we were unable to examine him. Parents are both unaffected, presuming recessive inheritance pattern. F - Canada Middle eastern origin - - Yes - retinal degeneration Fundus findings: Circumscribed central retinal atrophy (Retinal atrophy HP:0001105) Ocular coherence tomography (OCT): Atrophy of outer retina. Bruch's membrane is absent in the central fovea. Electroretinogram: Normal ffERG in the right eye; reduced cone flash and flicker in the left eye (Abnormal ERG HP:0000512) 1 2 Lance P Doucette
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