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Two 1p36 contiguous gene deletion syndromes are known so far: the terminal 1p36 deletion syndrome and a 1p36 deletion syndrome with a critical region located more proximal at 1p36.23-1p36.22. We present even more proximally located overlapping deletions from seven individuals, with the smallest region of overlap comprising 1 Mb at 1p36.13-1p36.12 (chr1:19077793-20081292 (GRCh37/hg19)) defining a new contiguous gene deletion syndrome. The characteristic features of this new syndrome are learning disability or mild intellectual disability, speech delay, behavioral abnormalities, and ptosis. The genes UBR4 and CAPZB are considered the most likely candidate genes for the features of this new syndrome.

Original publication

DOI

10.1111/cge.13739

Type

Journal article

Journal

Clin Genet

Publication Date

06/2020

Volume

97

Pages

927 - 932

Keywords

behavioral abnormality, chromosome deletion, chromosomes, human, learning disability, pair 1, ptosis, Blepharoptosis, Calmodulin-Binding Proteins, CapZ Actin Capping Protein, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 1, Developmental Disabilities, Female, Genetic Association Studies, Humans, Intellectual Disability, Learning Disabilities, Male, Phenotype, Ubiquitin-Protein Ligases