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Article

A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype.

The Turkish journal of pediatrics - 1 Jan 2000

Simşek-Kiper Pelin Ozlem, Utine Gülen Eda, Alanay Yasemin, Aktaş Dilek, Alikaşifoğlu Mehmet, Boduroğlu Koray

Abstract excerpt

Chromosome 2q37 microdeletion syndrome is a rare disorder characterized by mild-moderate psychomotor and growth retardation, autistic-like behavior, Albright hereditary osteodystrophy-like metacarpal/metatarsal shortening, and facial characteristics. We here report on a patient with 2q37 microdeletion presenting with learning difficulty, hyperactivity and attention deficit. Physical examination revealed...

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PMID: 22272459

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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