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De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature
- Source :
- European Journal of Medical Genetics. 55:117-119
- Publication Year :
- 2012
- Publisher :
- Elsevier BV, 2012.
-
Abstract
- Patients with distal deletions of chromosome 1q have a recognizable syndrome that includes microcephaly, hypoplasia or agenesis of the corpus callosum, and psychomotor retardation. Although these symptoms have been attributed to deletions of 1q42-1q44, the minimal chromosomal region involved has not yet defined. In this report, we describe a 7 years old male with mental retardation, cryptorchid testes, short stature and alopecia carrying only an interstitial de novo deletion of 911 Kb in the 1q43 region (239,597,095-240,508,817) encompassing three genes CHRM3, RPS7P5 and FMN2.
- Subjects :
- Male
Microcephaly
Chromosome 1
Deletion
Mental retardation
Genetics
Genetics (clinical)
Dwarfism
Biology
Short stature
Genetic
Intellectual Disability
medicine
Humans
Child
Agenesis of the corpus callosum
Gene
Sequence Deletion
Psychomotor retardation
Chromosome
General Medicine
medicine.disease
Hypoplasia
Chromosomes, Human, Pair 1
Chromosomal region
medicine.symptom
Subjects
Details
- ISSN :
- 17697212
- Volume :
- 55
- Database :
- OpenAIRE
- Journal :
- European Journal of Medical Genetics
- Accession number :
- edsair.doi.dedup.....03d6f71b8ccb02e866ea981197d89a5c