All individuals with variants in gene CNPY3

2 entries on 1 page. Showing entries 1 - 2.
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00301706 16-3145 PubMed: Maddirevula 2019 - F - - - - - - - ? intractable epilepsy, infantile spasm, laryngomalacia, hypotonia, brain atrophy, developmental delay and GERD and she is on NGT feeding. She cannot support and is dysmorphic (hairy forehead, short philtrum, low set ears, micrognathia) and has strabismus. The parents are first cousin once removed. They have another similarly affected daughter (6 months old). 1 1 Johan den Dunnen
00387729 M216 PubMed: Hu 2019 family, 3 affected individuals - - Iran Persia - - - - ID non-syndromic intellectual disability, no microcephaly 1 3 Johan den Dunnen
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