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Skeletal Dysplasia Conference, Children's Hospital, Nebraska
Sep 9
Skeletal Dysplasia Conference, Children's Hospital, Nebraska

The Jansen’s Foundation hosts first ever Skeletal Dysplasia Conference in Nebraska

Healing Beyond the Diagnosis - TJF at Amicus Therapeutics
Jun 7
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The Jansen’s Foundation visits Amicus Therapeutics for the Healing Beyond the Diagnosis initiative.

Rare Disease Day Proclaimed in Nebraska!
Feb 28
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Rare Disease Day Proclaimed in Nebraska!
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Rare Disease Day takes place on the last day of February each year. The main objective of Rare Disease Day is to raise awareness amongst the general public and decision-makers about rare disease and their impact on patient’s lives.

 
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Levi Krystosek's photograph among 2024 Rare Artist Contest Awardees

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9-year-old boy battling rare bone disease gets gift of a lifetime
9-year-old boy battling rare bone disease gets gift of a lifetime
Two Disabled Dudes Podcast: Live from Global Genes
Two Disabled Dudes Podcast: Live from Global Genes
 
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壁虎加速器破解版-hammer加速器

Jansen’s metaphyseal chondrodysplasia (JMC) is an extremely rare skeletal dysplasia characterized by progressive
growth plate abnormalities that affect most of the long bones.

 JMC is usually diagnosed during childhood, based on a combination of radiographic and biochemical abnormalities. However, some patients are not diagnosed until adulthood.

The limbs of affected individuals typically show progressive changes that are caused by an abnormal regulation of chondrocyte growth and differentiation, eventually leading to short and bowed legs. X-rays during infancy show demineralization and rickets-like metaphyseal changes. Fraying of the metaphyses is seen during childhood. Long bones do not grow normally and result in severely reduced adult height.

There is usually severe hypercalcemia and hypophosphatemia despite normal or undetectable serum levels of PTH or PTHrP.

Four different mutations in the gene encoding the PTH/PTHrP receptor (PTHR1) have been identified in several unrelated Jansen's patients. 

There are, at present, about 30 genetically confirmed cases of JMC, worldwide.  Six of these cases are living here in America.

 
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