Research Notes on Chondrodysplasia Punctata
Chondrodysplasia punctata is a rare, genetic skeletal disorder characterized by shortening of limbs and affecting infants and young children. There are different classifications of chondrodysplasia punctata, which depends on the pattern of inheritance (Autosomal or X-linked) that can predict the outcome of the disease. Genetic counseling is important to determine the form of chondrodysplasia punctata that occurs in the family.
Top Resources on Chondrodysplasia Punctata
- The Tyler Medical Clinic: Chondrodysplasia Punctata
- Stevensorenson.com: Chondrodysplasia Punctata
- TheFetus.net: Chondrodysplasia Punctata
- Orphanet: X-Linked Dominant Chondrodysplasia Punctata
- HON Select: Chondrodysplasia Punctata
- Encyclopædia Britannica: Chondrodysplasia Punctata (Pathology)
- About.com: Chondrodysplasia Punctata
- PubMed: Chondrodysplasia Punctata With A Mild Clinical Course
- InformaWorld: The Nature Of Cartilage Stippling In Chondrodysplasia Punctata
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About this WisdomCard
- Contributor: Madeleine Paladar
- Reviewer: Elisa Carter
- Supervised by: The OrganizedWisdom Physician Review Team
- Last update: Jul. 30, 2008
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