Age Dependent Progression of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Due to Heterozygous Mutations in COMP Gene
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
Grantová podpora
PRIMUS/17/MED/6
Univerzita Karlova v Praze
RVO VFN 64165
Ministerstvo Zdravotnictví Ceské Republiky
Progres Q32
Univerzita Karlova v Praze
PubMed
33030144
DOI
10.14712/23362936.2020.14
PII: pmr_2020121030153
Knihovny.cz E-zdroje
- Klíčová slova
- COMP, Multiple epiphyseal dysplasia, Pseudoachondroplasia, Short stature,
- MeSH
- achondroplazie MeSH
- chrupavkový oligomerní matrixový protein * genetika MeSH
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- matriliny genetika MeSH
- mutace * MeSH
- osteochondrodysplazie * diagnostické zobrazování genetika MeSH
- předškolní dítě MeSH
- retrospektivní studie MeSH
- stupeň závažnosti nemoci MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- předškolní dítě MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- chrupavkový oligomerní matrixový protein * MeSH
- COMP protein, human MeSH Prohlížeč
- matriliny MeSH
Dominantly inherited mutations in COMP gene encoding cartilage oligomeric matrix protein may cause two dwarfing skeletal dysplasias, milder multiple epiphyseal dysplasia (MED) and more severe pseudoachondroplasia (PSACH). We studied the phenotype and X-rays of 11 patients from 5 unrelated families with different COMP mutations. Whole exome and/or Sangers sequencing were used for molecular analyses. Four to ten X-ray images of hands hips, knees or spine were available for each patient for retrospective analyses. Eight patients with MED have mutation c.1220G>A and 3 children with PSACH mutations c.1359C>A, c.1336G>A, or the novel mutation c.1126G>T in COMP. Progressive failure in growth developed in all patients from early childhood and resulted in short stature < 3rd percentile in 7 patients and very short stature < 1st percentile in four. Most patients had joint pain since childhood, severe stiffness in shoulders and elbows but increased mobility in wrists. Six children had bowlegs and two had knock knees. In all patients, X-rays of hands, hips and knees showed progressive, age-dependent skeletal involvement more pronounced in the epiphyses of long rather than short tubular bones. Anterior elongation and biconvex configuration of vertebral bodies were more conspicuous for kids. Six children had correction of knees and two adults had hip replacement. Skeletal and joint impairment in patients with MED and PSACH due to COMP mutation start in early childhood. Although the clinical severity is mutation and age dependent, many symptoms represent a continuous phenotypic spectrum between both diseases. Most patients may benefit from orthopaedic surgeries.
Citace poskytuje Crossref.org