Growth Hormone Insensitivity

Dr. Ayush PandeyMBBS,PG Diploma

December 03, 2018

March 06, 2020

Growth Hormone Insensitivity
Growth Hormone Insensitivity

What is growth hormone insensitivity?

Growth hormone insensitivity (also known as Laron syndrome) or GHI is a very rare disease, wherein the body is not capable of fully utilizing the available growth hormone which is being produced by the pituitary gland. Growth hormone is responsible for physical growth (including height) of the body. So, insensitivity to growth hormone results in short stature or dwarfism.

What are its main signs and symptoms?

Growth hormone is the hormone responsible for physical growth and height of the body. Insensitivity to this growth hormone results in symptoms like that of growth hormone deficiency and are manifested poor physical growth and dwarfism.

Symptoms of GHI include:

  • Dwarfism or short height (Males < 1.35 meters and Females < 1.20 meters)
  • Poor muscle strength as well as muscle endurance
  • Delayed puberty
  • Low sugar levels (hypoglycaemia)
  • Small genitals
  • Short arms and legs
  • Obesity
  • Hair become thin and fragile
  • Facial features – sunken nasal ridge and protruding forehead

What are its main causes?

GHI usually happens due to modifications (mutation) in the genes that are passed on from parents to children and which affect the growth hormone receptor proteins on the body cells. This mutation in the growth hormone receptors results in poor response to this hormone, which, in turn, causes disruption of normal development and growth of body cells. This is also responsible for poor production of insulin-like growth factor, which helps in the growth of the body.

How is it diagnosed and treated?

A proper medical history with detailed family history and an adequate medical examination usually hints at the diagnosis. Certain blood investigations help in concluding the diagnosis, which includes:

  • Growth hormone levels – GH levels are high
  • Insulin-like growth factor levels –levels are low
  • GHR gene studies – It is a confirmatory test. It helps in checking for gene abnormality for the gene that codes for growth hormone receptor protein.

Treatment options for GHI include:

Currently, there is no curative treatment available for growth hormone insensitivity; however, certain drugs help in managing the signs and symptoms of GHI. These medications include:

  • Oral Medications – Mecasermin and Mecasermin rinfabate help in neutralizing the antibodies that are made against growth hormone receptors and reduce the intensity of symptoms
  • Injectable medications – Injecting insulin-like growth factor helps in growth and maturation of cells and improves body’s metabolism.



References

  1. National Organization for Rare Disorders. [Internet]. Danbury; Growth Hormone Insensitivity
  2. Soumik Goswami, Sujoy Ghosh, and Subhankar Chowdhury. Growth hormone insensitivity syndrome: A sensitive approach. Indian J Endocrinol Metab. 2012 Sep-Oct; 16(5): 817–818. PMID: 23087871
  3. Rosenfeld RG, Rosenbloom AL, Guevara-Aguirre J (1994). Growth hormone (GH) insensitivity due to primary GH receptor deficiency.. Endocr Rev 15:369–390.CrossRefPubMedWeb of ScienceGoogle Scholar
  4. Guevara-Aguirre J, Rosenbloom AL, Fielder PJ, Diamond Jr FB, Rosenfeld RG (1993). Growth hormone receptor deficiency in Ecuador: clinical and biochemical phenotype in two populations.. J Clin Endocrinol Metab 76:417–423
  5. Buchanan CR, Maheshwari HG, Norman MR, Morrell DJ, Preece MA. Clin Endocrinol (Oxf). Laron-type dwarfism with apparently normal high affinity serum growth hormone-binding protein.. 1991 Aug;35(2):179-85. PMID: 1934534

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