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Results 11 - 20 of 219 for Growth abnormality
  1. LRP5 gene 
    ... some cases, these conditions can cause abnormal bone growth and related skeletal abnormalities. Rarely, affected individuals have hearing loss or circulation ...
    https://medlineplus.gov/genetics/gene/lrp5 - Genetics
  2. AKT3 gene 
    ... However, unlike the mutations that cause those other abnormalities of brain growth, the genetic changes related to isolated hemimegalencephaly are ...
    https://medlineplus.gov/genetics/gene/akt3 - Genetics
  3. COL11A1 gene 
    ... with fibrochondrogenesis type 1, a disorder of bone growth characterized by severe skeletal abnormalities, hearing loss, and vision loss. Infants with fibrochondrogenesis ...
    https://medlineplus.gov/genetics/gene/col11a1 - Genetics
  4. IFT80 gene 
    ... the Sonic Hedgehog pathway, which may underlie the abnormalities of bone growth characteristic of asphyxiating thoracic dystrophy.In some affected individuals, asphyxiating thoracic dystrophy is also associated with abnormalities of the kidneys, liver, retinas, and other tissues. ...
    https://medlineplus.gov/genetics/gene/ift80 - Genetics
  5. DYNC2H1 gene 
    ... the Sonic Hedgehog pathway, which may underlie the abnormalities of bone growth characteristic of asphyxiating thoracic dystrophy.In some affected individuals, asphyxiating thoracic dystrophy is also associated with abnormalities of the kidneys, liver, retinas, and other tissues. ...
    https://medlineplus.gov/genetics/gene/dync2h1 - Genetics
  6. LEMD3 gene 
    ... the body.) The condition is characterized by skin growths called connective tissue nevi and bone abnormalities, most commonly osteopoikilosis. Osteopoikilosis refers to small, round ...
    https://medlineplus.gov/genetics/gene/lemd3 - Genetics
  7. MAP2K1 gene 
    ... created to replace it. These changes in bone growth and turnover underlie the bone abnormalities characteristic of melorheostosis. More About This Health Condition ...
    https://medlineplus.gov/genetics/gene/map2k1 - Genetics
  8. CDKN1C gene 
    ... genital anomalies. The condition is characterized by slow growth before and after birth, skeletal abnormalities, and hormonal changes. IMAGe syndrome occurs only when ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  9. PIK3R2 gene 
    ... mutation (in cases of mosaicism) help determine which abnormalities of brain growth will occur. p85 p85-BETA P85B phosphatidylinositol 3- ...
    https://medlineplus.gov/genetics/gene/pik3r2 - Genetics
  10. FLNA gene 
    ... important processes involved in skeletal development and cell growth, leading to the bone and skin abnormalities characteristic of terminal osseous dysplasia. More About This ...
    https://medlineplus.gov/genetics/gene/flna - Genetics
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