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  2. Achondroplasia in children - Wikipedia

    en.wikipedia.org/wiki/Achondroplasia_in_children

    Achondroplasia in children is the most common form of dwarfism; it accounts for about 70% of all cases of dwarfism. [1] Achondroplasia falls into the category of “disproportionate dwarfism”. It is linked to a mutation in the fibroblast growth factor receptor-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

    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).

  5. Silver–Russell syndrome - Wikipedia

    en.wikipedia.org/wiki/Silver–Russell_syndrome

    Silver–Russell syndrome, also called Silver–Russell dwarfism, is a rare congenital growth disorder. In the United States it is usually referred to as Russell–Silver syndrome, and Silver–Russell syndrome elsewhere. It is one of 200 types of dwarfism and one of five types of primordial dwarfism.

  6. Seckel syndrome - Wikipedia

    en.wikipedia.org/wiki/Seckel_syndrome

    Seckel syndrome, or microcephalic primordial dwarfism (also known as bird-headed dwarfism, Harper's syndrome, Virchow–Seckel dwarfism and bird-headed dwarf of Seckel [1]) is an extremely rare congenital nanosomic disorder. Inheritance is autosomal recessive. [2]

  7. Robinow syndrome - Wikipedia

    en.wikipedia.org/wiki/Robinow_syndrome

    Robinow syndrome is an extremely rare genetic disorder characterized by short-limbed dwarfism, abnormalities in the head, face, and external genitalia, as well as vertebral segmentation.

  8. Hypochondroplasia - Wikipedia

    en.wikipedia.org/wiki/Hypochondroplasia

    Hypochondroplasia (HCH) is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene that results in a disproportionately short stature, micromelia [3] and a head that appears large in comparison with the underdeveloped portions of the body.

  9. Psychosocial short stature - Wikipedia

    en.wikipedia.org/wiki/Psychosocial_short_stature

    Psychosocial short stature (PSS) is a growth disorder that is observed between the ages of 2 and 15, caused by extreme emotional deprivation or stress.. The symptoms include decreased growth hormone (GH) and somatomedin secretion, very short stature, weight that is inappropriate for the height, and immature skeletal age.