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

Sleep & breathing = Schlaf & Atmung - 1 Dec 2011

Al Saadi Muslim Mohammed

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Autonomic Nervous System
Chromosome Aberrations
Chromosomes, Human, Pair 4
Genetic Carrier Screening
Homeobox Protein PITX2
Hypoventilation
Saudi Arabia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Sleep Apnea, Central

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PMID: 21088916
DOI: 10.1007/s11325-010-0438-0

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Click a neighbor to travelStep 1 · 12 closest

Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report.PMID 21088916Read ↗

PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome.Semantic proximity Read ↗

Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report.Semantic proximity Read ↗

Adult With PHOX2B Mutation and Late-Onset Congenital Central Hypoventilation SyndromeSemantic proximity Read ↗

Genetic study of a patient with congenital central hypoventilation syndrome in Iran: a case report.Semantic proximity Read ↗

Congenital central hypoventilation syndrome: diagnosis and management.Semantic proximity Read ↗

A case of congenital central hypoventilation syndrome with PHOX2B gene mutation in a Korean neonate.Semantic proximity Read ↗

Central hypoventilation with PHOX2B expansion mutation presenting in adulthood.Semantic proximity Read ↗

PHOX2B gene mutation in a patient with late-onset central hypoventilation.Semantic proximity Read ↗

Genetic study of apatient with congenital central hypoventilation syndrome in Iran: a case reportSemantic proximity Read ↗

Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation.Semantic proximity Read ↗

Significant phenotype variability of congenital central hypoventilation syndrome in a family with polyalanine expansion mutation of the PHOX2B gene.Semantic proximity Read ↗

An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.Semantic proximity Read ↗

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