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Article

[Primary ciliary dyskinesia with HYDIN gene mutations in a child and literature review].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Apr 2017

Chen L L, Yang Y G, Wu J Z, Chen X R

Abstract excerpt

Objective: To review children's primary ciliary dyskinesia (PCD) in the pathogenesis, clinical manifestation, diagnosis and treatment. Method: To summarize and analyze the clinical data of a patient who was admitted to the first affiliated hospital of Xiamen University with primary ciliary dyskinesia in April 2014 while referring to related literature. Result: An 11 years old boy, weighting about 22 kg, had a...

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Source

Identifiers

PMID: 28441829
DOI: 10.3760/cma.j.issn.0578-1310.2017.04.014

Genes

HYDIN

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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