The state of Sergipe contribution to GH research: from Souza Leite to Itabaianinha syndrome

被引:7
作者
Aguiar-Oliveira, Manuel H. [1 ,3 ]
Salvatori, Roberto [2 ]
机构
[1] Univ Fed Sergipe, Div Endocrinol, Programa Posgrad Ciencias Saude, Aracaju, SE, Brazil
[2] Johns Hopkins Univ, Sch Med, Dept Med, Div Endocrinol Diabet & Metab, Baltimore, MD USA
[3] Univ Fed Sergipe, Hosp Univ, Div Endocrinol, Rua Claudio Batista S-N, BR-49060100 Aracaju, SE, Brazil
来源
ARCHIVES OF ENDOCRINOLOGY METABOLISM | 2022年 / 66卷 / 06期
关键词
GH; GHRH receptor; IGF1; acromegaly; growth hormone deficiency; GROWTH-HORMONE DEFICIENCY; HOMOZYGOUS MUTATION; RECEPTOR MUTATION; ADULT SUBJECTS; LIFETIME; MORPHOLOGY; MICRORNAS; INDIVIDUALS; SOMATOMEDIN; BINDING;
D O I
10.20945/2359-3997000000567
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the late 19th century, Jose Dantas de Souza Leite, a physician born in Sergipe, published the first detailed clinical description of acromegaly under the guidance of the French neurologist Pierre Marie. In 2014, the Brazilian Society of Endocrinology and Metabolism created the "Jose Dantas de Souza Leite Award", which is granted every two years to a Brazilian researcher who has contributed to the development of endocrinology. In 2022, the award was given to another physician from Sergipe, Manuel Herminio de Aguiar Oliveira, from the Federal University of Sergipe for the description of "Itabaianinha syndrome" in a cohort of individuals with isolated GH deficiency due to a homozygous inactivating mutation in the GH-releasing hormone receptor gene. This research, which was carried out over almost 30 years, was performed in partnership with Roberto Salvatori from Johns Hopkins University and in collaboration with other researchers around the world. This review article tells the story of Souza Leite, some milestones in the history of GH, and summarizes the description of Itabaianinha syndrome. Arch Endocrinol Metab. 2022;66(6):919-28
引用
收藏
页码:919 / 928
页数:10
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