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Growth patterns of young achondroplasia patients in Korea and predictability of neurosurgical procedures

DC Field Value Language
dc.contributor.authorLee, Jong Seok-
dc.contributor.authorShim, Youngbo-
dc.contributor.authorCho, Tae-Joon-
dc.contributor.authorKim, Seung-Ki-
dc.contributor.authorKo, Jung Min-
dc.contributor.authorPhi, Ji Hoon-
dc.date.accessioned2023-10-11T04:42:11Z-
dc.date.available2023-10-11T13:46:01Z-
dc.date.issued2023-10-05-
dc.identifier.citationOrphanet Journal of Rare Diseases, Vol.18(1):311ko_KR
dc.identifier.issn1750-1172-
dc.identifier.urihttps://hdl.handle.net/10371/195762-
dc.description.abstractBackground
Achondroplasia is an autosomal dominant disorder mainly affecting bony growth, typically resulting in markedly short stature. From a neurosurgical viewpoint, patients sometimes develop spinal cord compression at the narrowed foramen magnum and hydrocephalus. This study aims to construct growth references for height, weight, and head circumference (HC) of young achondroplasia patients in Korea and to evaluate the predictability of the necessity and timing of neurosurgical procedures through growth patterns.

Methods
Growth data were collected from achondroplasia patients who visited our institution between January 2002 and August 2022. First, we constructed percentile growth curves of height, weight, and HC for the patients under 3 years of age with the generalized additive model for location, scale, and shape (GAMLSS). Second, the growth patterns of the patients with hydrocephalus who underwent neurosurgical procedures such as foramen magnum decompression (FMD) and ventriculoperitoneal (VP) shunt were analyzed.

Results
There were 125 achondroplasia patients, including 67 males and 58 females. Among 125 patients, 46 underwent FMD, and 5 underwent VP shunt. As short stature and macrocephaly were typical characteristics of achondroplasia, the height of achondroplasia was lower than that of the general population, and HC in achondroplasia showed accelerated growth postnatally. There were no significant changes in HC in hydrocephalus patients before they underwent neurosurgical procedures. The influence of hydrocephalus on the growth patterns of HC in achondroplasia seemed insignificant.

Conclusion
Growth references for height, weight, and HC in young achondroplasia patients were constructed. It is the first report of growth patterns of achondroplasia in Korea. Unlike other pediatric patients, the diagnosis of hydrocephalus and the necessity of neurosurgical procedures are hard to be predicted with HC in achondroplasia. Neuroimaging should be considered for achondroplasia patients with neurological symptoms.
ko_KR
dc.description.sponsorshipThis study was jointly supported by a grant from Creative-Pioneering Researchers Program through Seoul National University (No. 800-20210571; to Phi JH) and a grant from SNUH Kun-hee Lee Child Cancer & Rare Disease Project, Republic of Korea (No. 22 A-003-0100; to Phi JH)ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.subjectAchondroplasia-
dc.subjectHead circumference-
dc.subjectGrowth-
dc.subjectHydrocephalus-
dc.subjectForamen magnum decompression-
dc.subjectVentriculoperitoneal shunt-
dc.titleGrowth patterns of young achondroplasia patients in Korea and predictability of neurosurgical proceduresko_KR
dc.typeArticleko_KR
dc.identifier.doi10.1186/s13023-023-02929-6ko_KR
dc.citation.journaltitleOrphanet Journal of Rare Diseasesko_KR
dc.language.rfc3066en-
dc.rights.holderInstitut National de la Santé et de la Recherche Médicale (INSERM)-
dc.date.updated2023-10-08T03:11:49Z-
dc.citation.volume18ko_KR
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