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Quoted phrase not found in phrase index: "Congenital macroorchidism"
Page 1
Hepatomegaly and fatty liver disease secondary to central hypothyroidism in combination with macrosomia as initial presentation of IGSF1 deficiency syndrome.
Nikolaou M, Vasilakis IA, Marinakis NM, Tilemis FN, Zellos A, Lykopoulou E, Traeger-Synodinos J, Kanaka-Gantenbein C. Nikolaou M, et al. Hormones (Athens). 2023 Sep;22(3):515-520. doi: 10.1007/s42000-023-00468-0. Epub 2023 Jul 26. Hormones (Athens). 2023. PMID: 37493943 Review.
PURPOSE: IGSF1 deficiency syndrome (immunoglobulin superfamily member 1) is considered the most common sex-linked cause of secondary congenital hypothyroidism and is characterized by a wide variety of other clinical and biochemical features, including hypoprolactine …
PURPOSE: IGSF1 deficiency syndrome (immunoglobulin superfamily member 1) is considered the most common sex-linked cause of secondary cong …
Giant macroorchidism in congenital adrenal hyperplasia.
Zadik Z, Burundukov E, Zung A. Zadik Z, et al. J Pediatr Endocrinol Metab. 2009 Dec;22(12):1095-7. doi: 10.1515/jpem.2009.22.12.1095. J Pediatr Endocrinol Metab. 2009. PMID: 20333867 No abstract available.
Rare case of central congenital hypothyroidism due to a TSHbeta mutation presenting with macro-orchidism.
Karguppikar MB, Schoenmakers N, Khadilkar V, Khadilkar A. Karguppikar MB, et al. BMJ Case Rep. 2023 Nov 14;16(11):e252796. doi: 10.1136/bcr-2022-252796. BMJ Case Rep. 2023. PMID: 37963664
A male infant was brought to our paediatric endocrine unit with typical clinical features of congenital hypothyroidism (CH) and striking macro-orchidism. On evaluation, free T3, free T4 and thyroid stimulating hormone (TSH) were found to be low, suggestive of con …
A male infant was brought to our paediatric endocrine unit with typical clinical features of congenital hypothyroidism (CH) an …