17q21.31 Microdeletion associated with infantile spasms

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Patients with 17q21.31 microdeletions frequently have neurologic abnormalities, especially seizures. This report is of a child with a deletion in this location who developed infantile spasms, a seizure type not specifically described in this syndrome. FISH analysis of parental blood metaphases demonstrated that the deletions occurred de novo. The deleted region encompasses the previously defined critical region for the 17q21.31 microdeletion syndrome, and includes the gene encoding for corticotropin-releasing hormone receptor 1, a protein implicated in hyperexcitability, and potentially in infantile spasms. Treatment with ACTH led to spasm cessation, consistent with its expected repression of CRH levels, which should be augmented by CRHR1 deletion, although this response was transient.

Original languageEnglish (US)
Pages (from-to)59-61
Number of pages3
JournalEuropean Journal of Medical Genetics
Volume56
Issue number1
DOIs
StatePublished - Jan 2013

Fingerprint

Infantile Spasms
Seizures
Nervous System Malformations
Corticotropin-Releasing Hormone Receptors
Spasm
Metaphase
Adrenocorticotropic Hormone
Genes
Proteins
Therapeutics
Chromosome 17q21.31 Deletion Syndrome

Keywords

  • 17q21.31 Microdeletion syndrome
  • CNV
  • Copy number variant
  • Corticotropin releasing hormone factor
  • Corticotropin releasing hormone receptor
  • CRFR
  • CRHR
  • Infantile spasms
  • West syndrome

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

17q21.31 Microdeletion associated with infantile spasms. / Wray, Carter.

In: European Journal of Medical Genetics, Vol. 56, No. 1, 01.2013, p. 59-61.

Research output: Contribution to journalArticle

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