Dysostosis cleidocranialis: Difference between revisions
From WikiLectures
(added infobox) |
No edit summary |
||
Line 1: | Line 1: | ||
'''Dysostosis''' (dysplasia) '''cleidocranialis''' is an [[autosomal dominant inheritance|AD]] hereditary'''''disorder of desmogenous''''' (gum, calf, pelvis) and '''''enchondral''''' (arm, leg, spine) [[ossification]]. For example, actor Gaten Matarazzo (who played Dustin Henderson in Stranger Things) suffers from the disease. | '''Dysostosis''' (dysplasia) '''cleidocranialis''' is an [[autosomal dominant inheritance|AD]] hereditary'''''disorder of desmogenous''''' (gum, calf, pelvis) and '''''enchondral''''' (arm, leg, spine) [[ossification]]. For example, actor Gaten Matarazzo (who played Dustin Henderson in Stranger Things) suffers from the disease. | ||
Line 39: | Line 37: | ||
* [[scoliosis]], pectus excavatum, | * [[scoliosis]], pectus excavatum, | ||
* brachycephaly, | * brachycephaly, | ||
* poorly developed teeth ([[Teething|delayed eruption and replacement]] of teeth). | * poorly developed teeth ([[Teething|delayed eruption and replacement]] of teeth).{{Infobox|name=Dysostosis cleidocranialis|caption=Hypoplasia of clavicles, bell-shaped rib cage|image=https://upload.wikimedia.org/wikipedia/commons/thumb/b/bc/Cleidocranial.jpg/800px-Cleidocranial.jpg}} | ||
== X-ray image == | == X-ray image == |
Revision as of 19:11, 11 November 2023
Dysostosis (dysplasia) cleidocranialis is an AD hereditarydisorder of desmogenous (gum, calf, pelvis) and enchondral (arm, leg, spine) ossification. For example, actor Gaten Matarazzo (who played Dustin Henderson in Stranger Things) suffers from the disease.
Pathogenesis
- Mutation of the RUNX2 gene (runt related transcription factor 2, gene naming recommended by HGNC; former gene name CBFA1) → abnormal bone tissue produced.[1]
Clinical picture
It usually manifests itself in the first 2 years, typical symptoms are:
- Broad head, relatively small face with hypertelorism, vertical shoulders, narrow chest, dentition disorder, persistent fontanelles,
- aplasia/ hypoplasia of the clavicle,
- short stature[2]
- hypermobility of the arm girdle,
- neuromuscular disorders from the brachial plexus damage and agenesis of some chest muscles,
- scoliosis, pectus excavatum,
- brachycephaly,
- poorly developed teeth (delayed eruption and replacement of teeth).
Dysostosis cleidocranialis
Hypoplasia of clavicles, bell-shaped rib cage
X-ray image
- Defective clavicles(in the lateral and central part),
- delayed closrie of fontanelles and cranial sutures (as opposed to craniostenosis),
- possibly deformities of the chest, pelvis, scoliosis, spina bifida occulta.
Therapy
- Reconstruction of the clavicles is not recommended, sometimes decompression of the brachial plexus,
- coxa vara: valgus intertrochanteric osteotomy,
- strengthening of the muscles of the shoulder girdle: exercise, bandage,
- treatment of scoliosis.
Links
Related articles
- Achondroplasia
- Thanatophoric dwarfism
- Diastrophic dysplasia (diastrophic dwarfism)
- Spondyloepiphyseal dysplasia
- Apert syndrome (acrocephalosyndactyly)
- Osteogenesis imperfecta (osteopsathyrhosis,ossium fragility)
- Arthrogryposis multiplex congenita
Reference
- MENDOZA-LONDONO, Roberto and Brendan LEE. Cleidocranial Dysplasia [online]. [feeling. 2017-05-29]. < https://www.ncbi.nlm.nih.gov/books/NBK1513/ >.
- WANG, Jiangping, Xinwen HUANG, and Can LAI, et al. Clinical spectrum of cleidocranial dysplasia in a family with twins. Pediatr Int [online] . 2013, vol. 55, no. 3, pp. 392-5, also available from < https://www.ncbi.nlm.nih.gov/pubmed/23782374 >. ISSN 1442-200X.
Sources
- DUNGLE, P., et al. Orthopedics. 1st edition. Prague: Grada Publishing, 2005. ISBN 80-247-0550-8 .
- ↑ MENDOZA-LONDONO, Roberto – LEE, Brendan. Cleidocranial Dysplasia [online]. [cit. 2017-05-29]. <https://www.ncbi.nlm.nih.gov/books/NBK1513/>.
- ↑ WANG, Jiangping – HUANG, Xinwen – LAI, Can. Clinical spectrum of cleidocranial dysplasia in a family with twins. Pediatr Int [online]. 2013, y. 3, p. 392-5, Available from <https://www.ncbi.nlm.nih.gov/pubmed/23782374>. ISSN 1442-200X.