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2q23.1 microdeletion syndrome (disorder)
2q23.1 microdeletion syndrome
Monosomy 2q23.1
Pseudo-Angelman syndrome
The newly described syndrome includes severe intellectual deficit with pronounced speech delay, behavioral abnormalities including hyperactivity and inappropriate laughter, short stature and seizures. To date, fifteen patients have been reported. Dysmorphic features include microcephaly, wide and open mouth, a tented upper lip, and prominent incisors. The majority of cases present with stereotypic repetitive behavior, disturbed sleep pattern and a broad-based gait. Skeletal abnormalities include generalized brachydactyly with small hands and feet. The size of the deletions is variable the critical region includes a single gene, MBD5.
2q23.1-micodeletiesyndroom
Id719657001
StatusPrimitive
Associated morphologyPartial monosomy
Finding siteLong arm of chromosome
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyPartial monosomy
Finding siteChromosome pair 2
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ93.5
RuleTRUE
AdviceALWAYS Q93.5
CorrelationSNOMED CT source code to target map code correlation not specified