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Laron syndrome.

作者信息

Guleria S, Sharma J, Kaushik S L

机构信息

Department of Pediatrics, Dr. Rajendra Prasad Government Medical College, Kangra, Himachal Pradesh, India.

出版信息

J Postgrad Med. 2014 Jul-Sep;60(3):322-3. doi: 10.4103/0022-3859.138816.

DOI:10.4103/0022-3859.138816

PMID:25121377

Abstract

摘要

相似文献

Laron syndrome.

J Postgrad Med. 2014 Jul-Sep;60(3):322-3. doi: 10.4103/0022-3859.138816.

Epilogue: The future of Laron syndrome - The need for changes.

Growth Horm IGF Res. 2016 Jun;28:79-80. doi: 10.1016/j.ghir.2015.07.007. Epub 2015 Jul 30.

[Laron type dwarfism].

Nihon Rinsho. 2006 May 28;Suppl 1:94-7.

Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries.

Cardiovasc J Afr. 2019;30(2):e7-e8. doi: 10.5830/CVJA-2019-002. Epub 2019 Jan 22.

[Delayed growth with raised circulating growth hormone and incapacity to produce somatomedin (dwarfism of Laron type)].

Ann Pediatr (Paris). 1977 Jan;24(1):63-7.

Identification of a novel mutation in the human growth hormone receptor gene (GHR) in a patient with Laron syndrome.

J Pediatr Endocrinol Metab. 2007 Jul;20(7):825-31. doi: 10.1515/jpem.2007.20.7.825.

Endocrine assessment, molecular characterization and treatment of growth hormone insensitivity disorders.

Nat Clin Pract Endocrinol Metab. 2006 Jul;2(7):395-407. doi: 10.1038/ncpendmet0195.

Novel growth hormone receptor gene mutation in a patient with Laron syndrome.

J Pediatr Endocrinol Metab. 2010 Apr;23(4):407-14. doi: 10.1515/jpem.2010.064.

A 42-Year-Old Woman with Untreated Growth Hormone Insensitivity, Diabetic Retinopathy, and Gene Sequencing Identifies a Variant of Laron Syndrome.

Am J Case Rep. 2019 May 14;20:689-696. doi: 10.12659/AJCR.913178.

[Novel nonsense mutation (p.Y113X) in the human growth hormone receptor gene in a Brazilian patient with Laron syndrome].

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1264-71. doi: 10.1590/s0004-27302008000800010.

引用本文的文献

A novel GHR variant in the first patient of Indian origin with genetically proven growth hormone insensitivity.

Indian J Endocrinol Metab. 2022 Mar-Apr;26(2):190-191. doi: 10.4103/ijem.ijem_24_22. Epub 2022 Apr 29.

Role of the GH-IGF1 axis on the hypothalamus-pituitary-testicular axis function: lessons from Laron syndrome.

Endocr Connect. 2021 Aug 25;10(9):1006-1017. doi: 10.1530/EC-21-0252.

Erratum: Laron syndrome.

J Postgrad Med. 2020 Apr-Jun;66(2):118. doi: 10.4103/0022-3859.169761.

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Laron syndrome.

作者信息

Guleria S, Sharma J, Kaushik S L

机构信息

Department of Pediatrics, Dr. Rajendra Prasad Government Medical College, Kangra, Himachal Pradesh, India.

出版信息

J Postgrad Med. 2014 Jul-Sep;60(3):322-3. doi: 10.4103/0022-3859.138816.

DOI:10.4103/0022-3859.138816

PMID:25121377

Abstract

摘要

相似文献

Laron syndrome.

J Postgrad Med. 2014 Jul-Sep;60(3):322-3. doi: 10.4103/0022-3859.138816.

Epilogue: The future of Laron syndrome - The need for changes.

Growth Horm IGF Res. 2016 Jun;28:79-80. doi: 10.1016/j.ghir.2015.07.007. Epub 2015 Jul 30.

[Laron type dwarfism].

Nihon Rinsho. 2006 May 28;Suppl 1:94-7.

Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries.

Cardiovasc J Afr. 2019;30(2):e7-e8. doi: 10.5830/CVJA-2019-002. Epub 2019 Jan 22.

[Delayed growth with raised circulating growth hormone and incapacity to produce somatomedin (dwarfism of Laron type)].

Ann Pediatr (Paris). 1977 Jan;24(1):63-7.

Identification of a novel mutation in the human growth hormone receptor gene (GHR) in a patient with Laron syndrome.

J Pediatr Endocrinol Metab. 2007 Jul;20(7):825-31. doi: 10.1515/jpem.2007.20.7.825.

Endocrine assessment, molecular characterization and treatment of growth hormone insensitivity disorders.

Nat Clin Pract Endocrinol Metab. 2006 Jul;2(7):395-407. doi: 10.1038/ncpendmet0195.

Novel growth hormone receptor gene mutation in a patient with Laron syndrome.

J Pediatr Endocrinol Metab. 2010 Apr;23(4):407-14. doi: 10.1515/jpem.2010.064.

A 42-Year-Old Woman with Untreated Growth Hormone Insensitivity, Diabetic Retinopathy, and Gene Sequencing Identifies a Variant of Laron Syndrome.

Am J Case Rep. 2019 May 14;20:689-696. doi: 10.12659/AJCR.913178.

[Novel nonsense mutation (p.Y113X) in the human growth hormone receptor gene in a Brazilian patient with Laron syndrome].

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1264-71. doi: 10.1590/s0004-27302008000800010.

引用本文的文献

A novel GHR variant in the first patient of Indian origin with genetically proven growth hormone insensitivity.

Indian J Endocrinol Metab. 2022 Mar-Apr;26(2):190-191. doi: 10.4103/ijem.ijem_24_22. Epub 2022 Apr 29.

Role of the GH-IGF1 axis on the hypothalamus-pituitary-testicular axis function: lessons from Laron syndrome.

Endocr Connect. 2021 Aug 25;10(9):1006-1017. doi: 10.1530/EC-21-0252.

Erratum: Laron syndrome.

J Postgrad Med. 2020 Apr-Jun;66(2):118. doi: 10.4103/0022-3859.169761.