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  2. 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]

  3. Zvi Laron - Wikipedia

    en.wikipedia.org/wiki/Zvi_Laron

    A multidisciplinary, comprehensive, ambulatory treatment scheme for diabetes mellitus in children. Diabetes care. 1979;2:342-8 Eshet R, Laron Z, Pertzelan A, Arnon R, Dintzman M. Defect of human growth hormone receptors in the liver of two patients with Laron-type dwarfism.

  4. Glycogenic hepatopathy - Wikipedia

    en.wikipedia.org/wiki/Glycogenic_Hepatopathy

    Glycogenic hepatopathy [1] (also known as Mauriac syndrome [2]) is a rare complication of type 1 diabetes characterized by extreme liver enlargement due to glycogen deposition, along with growth failure and delayed puberty. It occurs in some children and adolescents with type 1 diabetes irrespective of their glycemic control.

  5. BioMarin's dwarfism therapy gets FDA nod for expanded use - AOL

    www.aol.com/news/u-fda-approves-expanded...

    (Reuters) -The U.S. health regulator on Friday approved the expanded use of BioMarin Pharmaceutical's once-daily injection to treat children under the age of 5 with the most common form of short ...

  6. Growth hormone deficiency - Wikipedia

    en.wikipedia.org/wiki/Growth_hormone_deficiency

    Treatment is by growth hormone replacement using synthetic human growth hormone. [1] The frequency of the condition is unclear. [2] Most cases are initially noticed in children. [1] The genetic forms of this disease are estimated to affect about 1 in 7,000 people. [3] Most types occur equally in males and females though males are more often ...

  7. 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.

  8. Congenital iodine deficiency syndrome - Wikipedia

    en.wikipedia.org/wiki/Congenital_iodine...

    Adult stature without treatment ranges from 100 to 160 cm (3 ft 3 in to 5 ft 3 in), depending on severity, sex, and other genetic factors. Other signs include thickened skin, hair loss, enlarged tongue, and a protruding abdomen. [6] In children, bone maturation and puberty are severely delayed.

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

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

    M&S rebrands Midget Gems to avoid offending people with dwarfism. Josie Clarke. January 13, 2022 at 4:58 AM.