All individuals with variants in gene STX1B

4 entries on 1 page. Showing entries 1 - 4.
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00050683 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) M - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, abnormality of the outer ear, prominent metopic ridge, narrow mouth, inferior vermis hypoplasia, delayed speech and language development 1 2 Johan den Dunnen
00375517 175255 - - F no - - - - - - GEFSP9 (+) Behavioral abnormality,(+) Depressivity,(+) Autistic behavior,(+) Impaired social interactions,(+) Diminished motivation,(+) Delayed speech and language development,(+) Global developmental delay,(+) Febrile seizure (within the age range of 3 months to 6 years),(+) Expressive language delay,(+) Fatigue,(+) Abnormal social behavior,(+) Neurodevelopmental abnormality,(+) Sound sensitivity,(+) Constitutional symptom,(+) Impairment in personality functioning,(+) Diminished ability to concentrate,(+) Seizure precipitated by febrile infection,(+) Abnormal emotion/affect behavior 1 1 Andreas Laner
00390025 3 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Pale and tilted optic disk associated to hypoplasia, tortuous retinal vessels, non-homogeneous macula 1 1 LOVD
00424212 208881 - - M - - - - - - - GEFSP9 Hyperactivity, Short attention span, Intellectual disability, Generalized-onset motor seizure, Delayed speech and language development 1 1 Andreas Laner
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