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  2. Dwarfism - Wikipedia

    en.wikipedia.org/wiki/Dwarfism

    Dwarfism is a condition of people and animals marked by unusually small size or short stature. [1] In humans, it is sometimes defined as an adult height of less than 147 centimetres (4 ft 10 in), regardless of sex; the average adult height among people with dwarfism is 120 centimetres (4 ft).

  3. Dwarfism, low-birth-weight type with unresponsiveness to ...

    en.wikipedia.org/wiki/Dwarfism,_low-birth-weight...

    Dwarfism, low-birth-weight type with unresponsiveness to growth hormone is a very rare genetic disorder which is characterized by developmental delays, intellectual disabilities, and other anomalies. Only 2 cases have been described in medical literature.

  4. Chondrodystrophy - Wikipedia

    en.wikipedia.org/wiki/Chondrodystrophy

    It is thought that chondrodystrophy [2] is caused by an autosomal, recessive allele.To avoid a potential "lethal dose", both parents can be genetically tested.If a child is conceived with another carrier the outcome may be lethal, or the child may suffer from chondrodystrophy or dwarfism. [3]

  5. Laron syndrome - Wikipedia

    en.wikipedia.org/wiki/Laron_syndrome

    Laron syndrome (LS), also known as growth hormone insensitivity or growth hormone receptor deficiency (GHRD), is an autosomal recessive disorder characterized by a lack of insulin-like growth factor 1 (IGF-1; somatomedin-C) production in response to growth hormone (GH; hGH; somatotropin). [6]

  6. Seckel syndrome - Wikipedia

    en.wikipedia.org/wiki/Seckel_syndrome

    It is believed to be caused by defects of genes on chromosome 3 and 18. One form of Seckel syndrome can be caused by mutation in the gene encoding the ataxia telangiectasia and Rad3-related protein which maps to chromosome 3q22.1–q24. This gene is central in the cell's DNA damage response and repair mechanism.

  7. 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]

  8. M&S rebrands item to avoid offending people with dwarfism - AOL

    www.aol.com/m-rebrands-midget-gems-avoid...

    Marks and Spencer has changed the name of its popular Midget Gems sweets to avoid offending people with dwarfism. The retailer has rebranded its version of the confectionery as Mini Gems following ...

  9. Spondyloepiphyseal dysplasia congenita - Wikipedia

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

    This type of dwarfism is characterized by a normal spinal column length relative to the femur bone. Adult height ranges from 0.9 meters (35 inches) to just over 1.4 meters (55 inches). Curvature of the spine (such as kyphoscoliosis and lordosis) progresses during childhood and can