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- ...ane receptor, and it is a member of the [[cytokine receptor]] family. This receptor is found on the cell membrane of many types of tissues and organs, includin ...n]], a hormone produced by adipose tissue. When leptin binds to the leptin receptor, it activates a signaling pathway that results in the suppression of appeti2 KB (281 words) - 06:04, 29 February 2024
- '''Other Names:''' Obesity due to congenital leptin deficiency; Leptin deficiency or dysfunction; LEPD; Obesity, morbid, nonsyndromic 1 Congenital leptin deficiency is a form of monogenic obesity characterised by severe early-onset [[obesit6 KB (817 words) - 11:31, 24 October 2020
- * '''[[OAT deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/gyrate-atrophy-of-the-choro ...//ghr.nlm.nih.gov/condition/congenital-leptin-deficiency Congenital leptin deficiency]'''26 KB (3,308 words) - 20:59, 18 March 2024
- ...xin type 1 (PCSK1), or [[Leptin receptor deficiency|leptin receptor (LEPR) deficiency]], to help them lose weight and keep the weight off. ...xin type 1 (PCSK1), or [[Leptin receptor deficiency|leptin receptor (LEPR) deficiency]], to help them lose weight and keep the weight off.7 KB (1,070 words) - 17:07, 28 June 2021
- ...o treat problems caused by not having enough leptin in your body ([[leptin deficiency]]). ...eat problems caused by not having enough [[leptin]] in your body ([[leptin deficiency]]) in people with congenital or acquired [[generalized lipodystrophy]].9 KB (1,390 words) - 12:09, 4 September 2021
- ...3-hydroxyacyl-coa-dehydrogenase-deficiency 3-hydroxyacyl-CoA dehydrogenase deficiency]''' ...eglycine-amidinotransferase-deficiency Arginine:glycine amidinotransferase deficiency]'''39 KB (4,959 words) - 20:58, 18 March 2024
- * '''[[11-beta-hydroxylase deficiency]]''' * '''[[17-alpha-hydroxylase deficiency]]'''12 KB (1,529 words) - 22:30, 18 September 2019
- * '''[[11-beta-hydroxylase deficiency]]''' * '''[[17-alpha-hydroxylase deficiency]]'''12 KB (1,484 words) - 17:06, 20 August 2021
- ...[[insulin]] resistance. The disorder is caused by mutations in the insulin receptor gene. Symptoms include growth abnormalities of the head, face and nails, al ...y include an enlargement of the genitalia and [[precocious puberty]] and a deficiency or absence of fat tissue. Because individuals with Rabson–Mendenhall synd11 KB (1,511 words) - 16:06, 9 September 2020
- * '''[[C1 esterase inhibitor deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/hereditary-angioedema Hered * '''[[C1 inhibitor deficiency]]''' see '''[https://ghr.nlm.nih.gov/condition/hereditary-angioedema Hered114 KB (14,485 words) - 20:56, 18 March 2024
- * '''[[Lactate dehydrogenase A deficiency]]''' * '''[[Lactate dehydrogenase B deficiency]]'''34 KB (4,570 words) - 03:30, 10 April 2022
- * [[LDL receptor]] * [[LRBA deficiency]]21 KB (1,902 words) - 06:32, 28 August 2022
- * '''[[Receptor Activator of Nuclear Factor-kappa B]]''' * '''[[Receptor Activity-Modifying Protein 1]]'''47 KB (6,272 words) - 03:46, 10 March 2024
- * '''[[LDL-Receptor Related Protein-Associated Protein]]''' * '''[[LDL-Receptor Related Proteins]]'''31 KB (4,062 words) - 03:45, 10 March 2024
- # [[LDL receptor]] # [[Leptin receptor]]27 KB (2,638 words) - 15:13, 26 August 2021
- * '''[[leptin]]''' - A hormone predominantly made by adipose cells and enterocytes in the * [[17β-Hydroxysteroid dehydrogenase III deficiency]]64 KB (5,730 words) - 04:51, 6 November 2023
- * [[11 beta-hydroxysteroid dehydrogenase type 2 deficiency]] * [[11-beta-hydroxylase deficiency]]154 KB (13,094 words) - 04:47, 5 November 2023
- * [[11 beta-hydroxysteroid dehydrogenase type 2 deficiency]] * [[11-beta-hydroxylase deficiency]]144 KB (13,060 words) - 11:47, 19 February 2024
- * '''[[11-beta-hydroxylase deficiency]]''' * '''[[17-alpha-hydroxylase deficiency]]'''138 KB (16,857 words) - 05:28, 19 March 2024
- * '''[[11-beta-hydroxylase deficiency]]''' * '''[[17-alpha-hydroxylase deficiency]]'''137 KB (17,056 words) - 17:46, 19 March 2024