Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Eur J Med Genet ; 62(1): 55-60, 2019 Jan.
Article in English | MEDLINE | ID: mdl-29753921

ABSTRACT

De novo variants of ASH1L, which encodes a histone methyltransferase, have been reported in a few patients with intellectual disability and autistic features. Here, we identified a novel de novo frame-shift variant, c.2422_2423delAAinsT which predicts p.(Lys808TyrfsTer40), in ASH1L in a patient with multiple congenital anomalies (MCA), fine motor developmental delay, learning difficulties, attention deficit hyperactivity disorder, sleep apnea, and scoliosis. This frame-shift variant is expected to result in loss-of-function. Our report provides further evidence to support loss-of-function alterations of ASH1L as causative for an emergent neurodevelopmental syndrome characterized by MCA, intellectual disability, and behavioral problems, and further delineates this genetic disorder.


Subject(s)
Abnormalities, Multiple/genetics , DNA-Binding Proteins/genetics , Developmental Disabilities/genetics , Loss of Function Mutation , Phenotype , Transcription Factors/genetics , Abnormalities, Multiple/pathology , Child , Developmental Disabilities/pathology , Histone-Lysine N-Methyltransferase , Humans , Male , Syndrome
SELECTION OF CITATIONS
SEARCH DETAIL
...