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  2. 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]

  3. 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. More than 250,000 people in the world are diagnosed with achondroplasia.

  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. Hypochondroplasia - Wikipedia

    en.wikipedia.org/wiki/Hypochondroplasia

    Treatment Special education, Laminectomy [ 1 ] Hypochondroplasia ( HCH ) is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene ( FGFR3 ) that results in a disproportionately short stature, micromelia [ 3 ] and a head that appears large in comparison with the underdeveloped ...

  6. Chondrodystrophy - Wikipedia

    en.wikipedia.org/wiki/Chondrodystrophy

    Over 100 specific skeletal dysplasias have been identified. Chondrodystrophy is found in all races and in both females and male and occurs in around one of every 25,000 children. Chondrodystrophy and achondroplasia are the most common forms of genetic hyaline disorders. [citation needed] Hyaline cartilage caps the long bones and the spinal ...

  7. Osteochondrodysplasia - Wikipedia

    en.wikipedia.org/wiki/Osteochondrodysplasia

    Achondroplasia is a type of autosomal dominant genetic disorder that is the most common cause of dwarfism. It is also the most common type of non-lethal osteochondrodysplasia or skeletal dysplasia. The prevalence is approximately 1 in 25,000 births. [6]

  8. Vosoritide - Wikipedia

    en.wikipedia.org/wiki/Vosoritide

    Vosoritide, sold under the brand name Voxzogo, is a medication used for the treatment of achondroplasia, [3] [4] [5] a genetic condition that causes severely short stature and disproportionate growth.

  9. Severe achondroplasia with developmental delay and acanthosis ...

    en.wikipedia.org/wiki/Severe_Achondroplasia_with...

    Achondroplasia is a form of short-limbed dwarfism. This type of dwarfism is caused by the inability of the cartilage of the skeleton to ossify and turn to bone. [ 5 ] Acanthosis nigricans is a skin condition in which areas of the skin is of a dark and velvety discoloration, often seen in the body folds and creases such as the armpits, groin ...