Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: Case report and review

Marja W. Wessels; Nicolette J. Den Hollander; Ronald R. De Krijger; Peter G.J. Nikkels; Helen Brandenburg; Raoul Hennekam; Patrick J. Willems

doi:10.1002/ajmg.a.20202

Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: Case report and review

Marja W. Wessels
, Nicolette J. Den Hollander
, Ronald R. De Krijger
, Peter G.J. Nikkels
, Helen Brandenburg
, Raoul Hennekam
, Patrick J. Willems

Research output: Contribution to journal › Review article › peer-review

22 Citations (Scopus)

Abstract

Chondrodysplasia punctata (CDP) is a heterogeneous condition mainly characterized by premature and ectopic calcification of cartilage. Many genetic and nongenetic causes have been described leading to a preliminar etiological classification into defects of peroxisomal metabolism, defects in cholesterol metabolism, and vitamin K (vit K) metabolism. However, numerous cases of CDP still remain unclassified. The difficulties in reaching a causal diagnosis are illustrated here by a 23-week-old fetus with nonrhizomelic CDP characterized by extensive cartilage stippling, brachyphalangy, and nasal hypoplasia.

Original language	English
Pages (from-to)	97-104
Number of pages	8
Journal	American Journal of Medical Genetics, Part A
Volume	120 A
Issue number	1
DOIs	https://doi.org/10.1002/ajmg.a.20202
Publication status	Published - 1 Jul 2003
Externally published	Yes

Keywords

Brachyphalangic type
Cartilage calcification
Chondrodysplasia punctata
Maternal lupus erythematosus
Prenatal diagnosis
Review
Stippling
Ultrasound
Vit K

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title = "Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: Case report and review",

abstract = "Chondrodysplasia punctata (CDP) is a heterogeneous condition mainly characterized by premature and ectopic calcification of cartilage. Many genetic and nongenetic causes have been described leading to a preliminar etiological classification into defects of peroxisomal metabolism, defects in cholesterol metabolism, and vitamin K (vit K) metabolism. However, numerous cases of CDP still remain unclassified. The difficulties in reaching a causal diagnosis are illustrated here by a 23-week-old fetus with nonrhizomelic CDP characterized by extensive cartilage stippling, brachyphalangy, and nasal hypoplasia.",

keywords = "Brachyphalangic type, Cartilage calcification, Chondrodysplasia punctata, Maternal lupus erythematosus, Prenatal diagnosis, Review, Stippling, Ultrasound, Vit K",

author = "Wessels, \{Marja W.\} and \{Den Hollander\}, \{Nicolette J.\} and \{De Krijger\}, \{Ronald R.\} and Nikkels, \{Peter G.J.\} and Helen Brandenburg and Raoul Hennekam and Willems, \{Patrick J.\}",

year = "2003",

month = jul,

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doi = "10.1002/ajmg.a.20202",

language = "English",

volume = "120 A",

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journal = "American Journal of Medical Genetics, Part A",

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TY - JOUR

T1 - Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata

T2 - Case report and review

AU - Wessels, Marja W.

AU - Den Hollander, Nicolette J.

AU - De Krijger, Ronald R.

AU - Nikkels, Peter G.J.

AU - Brandenburg, Helen

AU - Hennekam, Raoul

AU - Willems, Patrick J.

PY - 2003/7/1

Y1 - 2003/7/1

N2 - Chondrodysplasia punctata (CDP) is a heterogeneous condition mainly characterized by premature and ectopic calcification of cartilage. Many genetic and nongenetic causes have been described leading to a preliminar etiological classification into defects of peroxisomal metabolism, defects in cholesterol metabolism, and vitamin K (vit K) metabolism. However, numerous cases of CDP still remain unclassified. The difficulties in reaching a causal diagnosis are illustrated here by a 23-week-old fetus with nonrhizomelic CDP characterized by extensive cartilage stippling, brachyphalangy, and nasal hypoplasia.

AB - Chondrodysplasia punctata (CDP) is a heterogeneous condition mainly characterized by premature and ectopic calcification of cartilage. Many genetic and nongenetic causes have been described leading to a preliminar etiological classification into defects of peroxisomal metabolism, defects in cholesterol metabolism, and vitamin K (vit K) metabolism. However, numerous cases of CDP still remain unclassified. The difficulties in reaching a causal diagnosis are illustrated here by a 23-week-old fetus with nonrhizomelic CDP characterized by extensive cartilage stippling, brachyphalangy, and nasal hypoplasia.

KW - Brachyphalangic type

KW - Cartilage calcification

KW - Chondrodysplasia punctata

KW - Maternal lupus erythematosus

KW - Prenatal diagnosis

KW - Review

KW - Stippling

KW - Ultrasound

KW - Vit K

UR - https://www.scopus.com/pages/publications/0041321152

U2 - 10.1002/ajmg.a.20202

DO - 10.1002/ajmg.a.20202

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C2 - 12794700

AN - SCOPUS:0041321152

SN - 1552-4825

VL - 120 A

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EP - 104

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 1

ER -

Fetus with an unusual form of nonrhizomelic chondrodysplasia punctata: Case report and review

Abstract

Keywords

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