Cervical spine stenosis and possible vitamin K deficiency embryopathy in an unusual case of chondrodysplasia punctata and an updated classification system
- PMID: 12949976
- DOI: 10.1002/ajmg.a.20242
Cervical spine stenosis and possible vitamin K deficiency embryopathy in an unusual case of chondrodysplasia punctata and an updated classification system
Abstract
We describe in this paper a patient with brachytelephalangic chondrodysplasia punctata (BCDP) who has multiple serious medical problems and striking physical abnormalities. These include cervical spine stenosis with resultant quadriplegia, severe nasal hypoplasia, and brachytelephalangy. Radiographs taken shortly after birth demonstrated extensive epiphyseal and vertebral stippling, and distal phalangeal hypoplasia. The pregnancy was complicated by maternal intestinal obstruction due to a small bowel carcinoma and probable malabsorption. The severity of the phenotype in this case may have been influenced by these maternal factors particularly vitamin K deficiency.
Copyright 2003 Wiley-Liss, Inc.
Similar articles
-
Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolism.Am J Med Genet. 1997 Oct 17;72(2):129-34. Am J Med Genet. 1997. PMID: 9382132
-
Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata.Pediatr Radiol. 2018 Jul;48(7):979-991. doi: 10.1007/s00247-018-4098-8. Epub 2018 Mar 23. Pediatr Radiol. 2018. PMID: 29572747 Free PMC article.
-
Brachytelephalangic chondrodysplasia punctata with marked cervical stenosis and cord compression: report of two cases.Pediatr Radiol. 2002 Jun;32(6):452-6. doi: 10.1007/s00247-001-0638-7. Epub 2002 Feb 2. Pediatr Radiol. 2002. PMID: 12029348
-
Prenatal diagnosis of cervical spinal cord compression in chondrodysplasia punctata brachytelephalangic type: A case report and literature review.Congenit Anom (Kyoto). 2013 Dec;53(4):160-2. doi: 10.1111/cga.12003. Congenit Anom (Kyoto). 2013. PMID: 24712475 Review.
-
Chondrodysplasia punctata: case report and review of audiological and ENT features.J Laryngol Otol. 2006 Mar;120(3):233-6. doi: 10.1017/S002221510500472X. Epub 2005 Nov 25. J Laryngol Otol. 2006. PMID: 16359148 Review.
Cited by
-
Clinical and radiological pictures of two newborn babies with manifestations of chondrodysplasia punctata and review of available literature.Pol J Radiol. 2013 Apr;78(2):57-64. doi: 10.12659/PJR.883947. Pol J Radiol. 2013. PMID: 23807887 Free PMC article.
-
Successful Treatment of Atlantoaxial Subluxation in an Adolescent Patient with BrachytelephalangicChondrodysplasia Punctata.Case Rep Orthop. 2019 Jan 27;2019:5974281. doi: 10.1155/2019/5974281. eCollection 2019. Case Rep Orthop. 2019. PMID: 30809406 Free PMC article.
-
Kabuki Syndrome: Case Report of Severe Prenatal Midface Hypoplasia (Binder Phenotype), due to a Novel Variant in the KMT2D Gene.Mol Syndromol. 2025 Feb;16(1):38-42. doi: 10.1159/000540088. Epub 2024 Aug 8. Mol Syndromol. 2025. PMID: 39911174 Free PMC article.
-
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss.Mol Cytogenet. 2015 Oct 31;8:83. doi: 10.1186/s13039-015-0187-7. eCollection 2015. Mol Cytogenet. 2015. PMID: 26526591 Free PMC article.
-
Hand Radiographs in Skeletal Dysplasia: A Pictorial Review.Indian J Radiol Imaging. 2023 Dec 15;34(2):291-308. doi: 10.1055/s-0043-1777320. eCollection 2024 Apr. Indian J Radiol Imaging. 2023. PMID: 38549896 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases