Literature DB >> 22272459

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

Pelin Ozlem Simşek-Kiper1, Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş, Mehmet Alikaşifoğlu, Koray Boduroğlu.   

Abstract

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 psychomotor and growth retardation, facial dysmorphism and brachydactyly, suggestive of Albright hereditary osteodystrophy-like phenotype. Laboratory evaluation revealed 46, XX.ish subtel(2q)(D2S447-) confirming 2q37 microdeletion. Chromosome 2q37 microdeletion syndrome should be considered in the differential diagnosis of patients presenting with psychomotor and growth retardation and an Albright hereditary osteodystrophy-like phenotype, especially in the presence of brachydactyly, even if the characteristic facial features are missing.

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Year:  2011        PMID: 22272459

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  1 in total

1.  2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis.

Authors:  Eun-Kyung Cho; Jinsup Kim; Aram Yang; Sung Yoon Cho; Dong-Kyu Jin
Journal:  Ann Pediatr Endocrinol Metab       Date:  2017-06-28
  1 in total

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