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Article

A nonverbal learning disability in a case of central hypoventilation syndrome without a PHOX2B gene mutation.

Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence - 1 Jan 2010

Trobliger Robert, Zaroff Charles M, Grayson Richard H, Higgins Joseph J

Abstract excerpt

This study examines the neuropsychological profile of a boy with congenital central hypoventilation syndrome (CCHS) without a paired-like homeobox gene (PHOX2B) mutation. CCHS is a rare disorder of autonomic nervous system development characterized by an impaired ventilatory response to hypercarbia and hypoxemia. Mild intellectual deficits are common but a specific cognitive profile is not established in CCHS. We...

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Identifiers

PMID: 19813116
DOI: 10.1080/09297040903266897

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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