Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report

Journal article

Peer reviewed

Sleep & breathing, Vol.15(4), pp.875-878

01/12/2011

PMID: 21088916

Abstract

Alleles

Autonomic Nervous System - physiopathology

Chromosome Aberrations

Chromosomes, Human, Pair 4 - genetics

Cluster Analysis

DNA Mutational Analysis

Genes, Dominant - genetics

Genetic Carrier Screening

Homeodomain Proteins - genetics

Humans

Hypoventilation - diagnosis

Hypoventilation - genetics

Hypoventilation - therapy

Infant, Newborn

Male

Saudi Arabia

Sleep Apnea, Central - diagnosis

Sleep Apnea, Central - genetics

Sleep Apnea, Central - therapy

Transcription Factors - genetics

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Title: Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report
Creators - without role: Muslim Mohammed Al Saadi - King Saud University
Publication Details: Sleep & breathing, Vol.15(4), pp.875-878
Identifiers: 9947076008331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article