enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Achondroplasia in children - Wikipedia

    en.wikipedia.org/wiki/Achondroplasia_in_children

    Achondroplasia is defined by central nervous system defects as well as the prior physical symptoms. Average height for an adult man or woman diagnosed with achondroplasia is about 120 centimeters (47.2 inches), although technically a maximum of 148 centimeters (58.2 inches) is also considered achondroplastic. [3]

  3. Achondroplasia - Wikipedia

    en.wikipedia.org/wiki/Achondroplasia

    Achondroplasia is a genetic disorder with an autosomal dominant pattern of inheritance whose primary feature is dwarfism. [3] It is the most common cause of dwarfism [4] and affects about 1 in 27,500 people. [3] In those with the condition, the arms and legs are short, while the torso is typically of normal length. [3]

  4. Dwarfism - Wikipedia

    en.wikipedia.org/wiki/Dwarfism

    In men and women, the sole requirement for being considered a dwarf is having an adult height under 147 cm (4 ft 10 in) and it is almost always sub-classified with respect to the underlying condition that is the cause of the short stature. Dwarfism is usually caused by a genetic variant; achondroplasia is caused by a mutation on chromosome 4 ...

  5. Dwarfing - Wikipedia

    en.wikipedia.org/wiki/Dwarfing

    Shortened stature can result from growth hormone deficiency, starvation, portal systemic shunts, renal disease, hypothyroidism diabetes mellitus and other conditions. Any of these conditions can be established in a population through genetic engineering, selective breeding, or insular dwarfism, or some combination of the above.

  6. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    For example, the common form of dwarfism, achondroplasia, is typically considered a dominant disorder, but children with two genes for achondroplasia have a severe and usually lethal skeletal disorder, one that achondroplasics could be considered carriers for. Sickle cell anemia is also considered a recessive condition, but heterozygous ...

  7. Spondyloepiphyseal dysplasia congenita - Wikipedia

    en.wikipedia.org/wiki/Spondyloepiphyseal...

    Spondyloepiphyseal dysplasia congenita (abbreviated to SED more often than SDC) is a rare disorder of bone growth that results in dwarfism, [1] characteristic skeletal abnormalities, and, in some instances, problems with vision and hearing.

  8. Short stature - Wikipedia

    en.wikipedia.org/wiki/Short_stature

    When the cause is unknown, it is called idiopathic short stature. [5] Short stature can also be caused by the bone plates fusing at an earlier age than normal, therefore stunting growth. Normally, the bone age is the same as the biological age but for some people, it is older. For many people with advanced bone ages, they hit a growth spurt ...

  9. Growth hormone deficiency - Wikipedia

    en.wikipedia.org/wiki/Growth_hormone_deficiency

    In a third of cases no cause is apparent. [2] The underlying mechanism generally involves problems with the pituitary gland. [2] Some cases are associated with a lack of other pituitary hormones, in which case it is known as combined pituitary hormone deficiency. [4] Diagnosis involves blood tests to measure growth hormone levels. [2]