SHOX-related short stature

SHOX-related short stature is a primary bone dysplasia characterized by a height that is 2 standard deviations below the corresponding mean height for a given age, sex and population group, in the absence of obvious skeletal abnormalities and other diseases and with normal developmental milestones. Patients present normal bone age with normal limbs, shortening of the extremities (significantly lower extremities-trunk and sitting height-to-height ratios), normal hGH values, normal karyotype, and Leri-Weill dyschondrosteosis-like radiological signs (e.g. triangularization of distal radial epiphyses, pyramidalization of distal carpal row, and lucency of the distal radius on the ulnar side). Mesomelic disproportions and Madelung deformity are not apparent at a young age, but may develop later in life or never.



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Total: 0 (papers)

  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 16

HPO ID Term Frequency
HP:0000218 High palate Very frequent (99-80%)
HP:0000347 Micrognathia Very frequent (99-80%)
HP:0000470 Short neck Very frequent (99-80%)
HP:0001773 Short foot Very frequent (99-80%)
HP:0002650 Scoliosis Very frequent (99-80%)
HP:0002857 Genu valgum Very frequent (99-80%)
HP:0002967 Cubitus valgus Very frequent (99-80%)
HP:0002982 Tibial bowing Very frequent (99-80%)
HP:0003067 Madelung deformity Very frequent (99-80%)
HP:0003712 Skeletal muscle hypertrophy Very frequent (99-80%)
HP:0004322 Short stature Very frequent (99-80%)
HP:0005856 Ulnar radial head dislocation Very frequent (99-80%)
HP:0005974 Episodic ketoacidosis Very frequent (99-80%)
HP:0009816 Lower limb undergrowth Very frequent (99-80%)
HP:0009821 Forearm undergrowth Very frequent (99-80%)
HP:0001513 Obesity Frequent (79-30%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 1

Gene Symbol Gene Name Entrez Gene ID
SHOX short stature homeobox 6473