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Rabson-Mendenhall syndrome.
Gupta J, Daniel JM, Vasudevan V. Gupta J, et al. J Indian Soc Pedod Prev Dent. 2012 Jul-Sep;30(3):279-82. doi: 10.4103/0970-4388.105026. J Indian Soc Pedod Prev Dent. 2012. PMID: 23263437
Rabson-Mendenhall syndrome is a rare, autosomal recessive disorder affecting insulin receptor. ...Mutations of the insulin receptor gene affecting insulin action appear to be the basic mechanism underlying this syndrome. Herein, we present a case report on …
Rabson-Mendenhall syndrome is a rare, autosomal recessive disorder affecting insulin receptor. ...Mutations of the insu …
Rabson-Mendenhall syndrome.
Parveen BA, Sindhuja R. Parveen BA, et al. Int J Dermatol. 2008 Aug;47(8):839-41. doi: 10.1111/j.1365-4632.2008.03591.x. Int J Dermatol. 2008. PMID: 18717867
Rabson mendenhall syndrome is a rare autosomally recessive inherited insulin resistant disorder. ...We report a male patient with all the features of Rabson-Mendenhall syndrome from our institute....
Rabson mendenhall syndrome is a rare autosomally recessive inherited insulin resistant disorder. ...We report a male pa …
Early onset of diabetic nephropathy.
Francis J, Rose SJ, Raafat F, Milford DV. Francis J, et al. Arch Dis Child. 1997 Dec;77(6):524-5. doi: 10.1136/adc.77.6.524. Arch Dis Child. 1997. PMID: 9496190 Free PMC article.
A 12 year old Asian girl with a four year history of poorly controlled insulin dependent diabetes mellitus developed overt diabetic nephropathy. There were no clinical features of Rabson-Mendenhall syndrome. Screening for microalbuminuria would have identifie …
A 12 year old Asian girl with a four year history of poorly controlled insulin dependent diabetes mellitus developed overt diabetic nephropa …
Rabson-Mendenhall Syndrome in a brother-sister pair in Kuwait: Diagnosis and 5 year follow up.
Al-Kandari H, Al-Abdulrazzaq D, Al-Jaser F, Al-Mulla F, Davidsson L. Al-Kandari H, et al. Prim Care Diabetes. 2021 Feb;15(1):175-177. doi: 10.1016/j.pcd.2020.07.012. Epub 2020 Aug 23. Prim Care Diabetes. 2021. PMID: 32843252
AIM: To report on Rabson-Mendenhall Syndrome (RMS) diagnosed in Kuwait. METHODS: A toddler (18 months old) was referred with high plasma insulin and dysmorphic features suggestive of RMS including coarse facial features with globular nose, full lips and furro …
AIM: To report on Rabson-Mendenhall Syndrome (RMS) diagnosed in Kuwait. METHODS: A toddler (18 months old) was referred …
Rabson-Mendenhall syndrome: two case reports and a brief review of the literature.
Bathi RJ, Parveen S, Mutalik S, Rao R. Bathi RJ, et al. Odontology. 2010 Feb;98(1):89-96. doi: 10.1007/s10266-009-0106-7. Epub 2010 Feb 16. Odontology. 2010. PMID: 20155514 Review.
Rabson-Mendenhall syndrome is a rare, autosomal recessive disorder characterized by insulin resistance syndrome, growth retardation, coarse and senile-looking faces, mental precocity, early dentition, and pineal hyperplasia. Mutations of the insulin receptor …
Rabson-Mendenhall syndrome is a rare, autosomal recessive disorder characterized by insulin resistance syndrome, growth …
Management challenges of Rabson Mendenhall syndrome in a resource limited country: a case report.
Aftab S, Shaheen T, Asif R, Anjum MN, Saeed A, Manzoor J, Cheema HA. Aftab S, et al. J Pediatr Endocrinol Metab. 2022 Sep 16;35(11):1429-1432. doi: 10.1515/jpem-2022-0214. Print 2022 Nov 25. J Pediatr Endocrinol Metab. 2022. PMID: 36106528
OBJECTIVES: Rabson Mendenhall syndrome (RMS) is a rare form of insulin resistance syndrome caused by insulin receptor mutation. ...
OBJECTIVES: Rabson Mendenhall syndrome (RMS) is a rare form of insulin resistance syndrome caused by insulin receptor m …
Use of a Sodium-Glucose Cotransporter 2 Inhibitor, Empagliflozin, in a Patient with Rabson-Mendenhall Syndrome.
Dos Santos SS, Ramaldes LA, Gabbay MAL, Moises RCS, Dib SA. Dos Santos SS, et al. Horm Res Paediatr. 2021;94(7-8):313-316. doi: 10.1159/000519613. Epub 2021 Sep 22. Horm Res Paediatr. 2021. PMID: 34551418
INTRODUCTION: Among the insulin resistance syndromes that lead to diabetes mellitus in young people, Rabson-Mendenhall syndrome (RMS; OMIM # 262190) is an autosomal recessive inherited disease caused by an insulin receptor mutation (INSR; 147,670). ...
INTRODUCTION: Among the insulin resistance syndromes that lead to diabetes mellitus in young people, Rabson-Mendenhall synd …
A Novel Mutation in the INSR Gene Causes Severe Insulin Resistance and Rabson-Mendenhall Syndrome in a Paraguayan Patient.
Rojas Velazquez MN, Blanco F, Ayala-Lugo A, Franco L, Jolly V, Di Tore D, Martínez de Lapiscina I, Janner M, Flück CE, Pandey AV. Rojas Velazquez MN, et al. Int J Mol Sci. 2024 Mar 8;25(6):3143. doi: 10.3390/ijms25063143. Int J Mol Sci. 2024. PMID: 38542117 Free PMC article.
Rabson-Mendenhall syndrome (RMS) is a rare autosomal recessive disorder characterized by severe insulin resistance, resulting in early-onset diabetes mellitus. ...
Rabson-Mendenhall syndrome (RMS) is a rare autosomal recessive disorder characterized by severe insulin resistance, res …
One Novel 2.43Kb Deletion and One Single Nucleotide Mutation of the INSR Gene in a Chinese Neonate with Rabson-Mendenhall Syndrome.
Chen X, Wang H, Wu B, Dong X, Liu B, Chen H, Lu Y, Zhou W, Yang L. Chen X, et al. J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):183-187. doi: 10.4274/jcrpe.5080. Epub 2017 Oct 30. J Clin Res Pediatr Endocrinol. 2018. PMID: 29082893 Free PMC article.
Mutations in the insulin receptor (INSR) gene are responsible for Donohue syndrome (DS) and Rabson-Mendenhall syndrome (RMS). Insulin resistance is a feature of both diseases. Our patient was a Chinese neonate suffering from abnormal glucose homeostasis, hype …
Mutations in the insulin receptor (INSR) gene are responsible for Donohue syndrome (DS) and Rabson-Mendenhall syndrome …
23 results