Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Haddad syndrome.

Anaesthesiology intensive therapy - 1 Jan 2000

Ławicka Marzena, Sawicka Joanna, Bąkowska Grażyna

Abstract excerpt

Haddad syndrome is a rare genetically conditioned disease. We present a female newborn with congenital central hypoventilation syndrome associated with Hirschprung's disease. The infant is mechanically ventilated and parentally fed in a home setting. The diagnosis has been confirmed by the presen...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Homeodomain Proteins
Share to Hypoventilation
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Sleep Apnea, Central

Share to Transcription Factors

Source

Identifiers

PMID: 23572305
DOI: 10.5603/AIT.2013.0006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23572305-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Haddad syndrome.PMID 23572305Read ↗

Haddad syndrome with PHOX2B gene mutation in a Korean infant.Semantic proximity Read ↗

Case report of Haddad syndrome in a newborn: congenital central hypoventilation syndrome and Hirschsprung's disease.Semantic proximity Read ↗

Clinical practices and prognosis of Congenital Central Hypoventilation Syndrome : based on 20-year-records in KoreaSemantic proximity Read ↗

Congenital hypoventilation syndrome and Hirschsprung's disease - Haddad syndrome: A neonatal case presentation.Semantic proximity Read ↗

Guidelines for diagnosis and management of congenital central hypoventilation syndrome.Semantic proximity Read ↗

Central congenital hypoventilation syndrome: changing face of a less mysterious but more complex genetic disorder.Semantic proximity Read ↗

Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisions.Semantic proximity Read ↗

Congenital central hypoventilation syndrome: a bedside-to-bench success story for advancing early diagnosis and treatment and improved survival and quality of life.Semantic proximity Read ↗

The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.Semantic proximity Read ↗

Genotype-phenotype relationship in Japanese patients with congenital central hypoventilation syndrome.Semantic proximity Read ↗

Congenital central hypoventilation syndrome: four families.Semantic proximity Read ↗

Congenital central hypoventilation syndrome and the PHOX2B gene mutation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.