Descripción general de la clínica y el abordaje terapéutico | 23 AGO 22

Hipopituitarismo congénito

Revisión sobre el desarrollo normal de la hipófisis y las causas, la presentación clínica y los métodos de diagnóstico y manejo actuales del hipopituitarismo congénito
Autor/a: Geoanna Bautista Neoreviews (2022) 23 (5): e300e310
INDICE:  1. Texto principal | 2. Referencia bibliográfica
Referencia bibliográfica

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3. Alatzoglou KS, Dattani MT. Genetic forms of hypopituitarism and their manifestation in the neonatal period. Early Hum Dev. 2009; 85(11):705–712

4. Bosch I Ara L, Katugampola H, Dattani MT. Congenital hypopituitarism during the neonatal period: epidemiology, pathogenesis, therapeutic options, and outcome. Front Pediatr. 2021;8:600962

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30. Bonfig W, Krude H, Schmidt H. A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck-a case report and review of the literature. Eur J Pediatr. 2011;170(8): 1017–1021

31. Filges I, Bischof-Renner A, R€othlisberger B, et al. Panhypopituitarism presenting as life-threatening heart failure caused by an inherited microdeletion in 1q25 including LHX4. Pediatrics. 2012;129(2):e529–e534

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34. Mehta S, Brar PC. Severe, persistent neonatal hypoglycemia as a presenting feature in patients with congenital hypopituitarism: a review of our case series. J Pediatr Endocrinol Metab. 2019;32(7): 767–774

35. Piantanida E, Ippolito S, Gallo D, et al. The interplay between thyroid and liver: implications for clinical practice. J Endocrinol Invest. 2020;43(7):885–899

 

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