Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities

Thyroid

Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation

Front Endocrinol (Lausanne).

Majdoub H, Amselem S, Legendre M, Rath S, Bercovich D, Tenenbaum-Rakover Y

doi: 10.3389/fendo.2019.00381.

Hypogonadism

A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism

Front Endocrinol (Lausanne).

Indirli R, Cangiano B, Profka E, Mantovani G, Persani L, Arosio M, Bonomi M, Ferrante E

doi: 10.3389/fendo.2019.00781.

HypogonadismObesity and Bariatric Surgery

A boy with Prader-Willi syndrome: unmasking precocious puberty during growth hormone replacement therapy

Arch Endocrinol Metab.

Ludwig NG, Radaeli RF, Silva MM, Romero CM, Carrilho AJ, Bessa D, Macedo DB, Oliveira ML, Latronico AC, Mazzuco TL

doi: 10.1590/

Further Publications

Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH) and Subsequent Central Diabetes Insipidus: A Rare Presentation of Pituitary Apoplexy

Case Rep Endocrinol.

Smedegaard SB, Jørgensen JO, Rittig N

doi: 10.1155/2019/7592648.

Diabetes - GeneralGlycemic Control

Emergence of insulin resistance following empirical glibenclamide therapy: a case report of neonatal diabetes with a recessive INS gene mutation

J Pediatr Endocrinol Metab.

Yildiz M, Akcay T, Aydin B, Akgun A, Dogan BB, De Franco E, Ellard S, Onal H

doi: 10.1515/jpem-2017-0325.

Diabetes - GeneralGlycemic ControlObesity and Bariatric Surgery

Diagnostic and management challenges from childhood, puberty through to transition in severe insulin resistance due to insulin receptor mutations.

Pediatr Diabetes.

Wei C, Burren CP

doi: 10.1111/pedi.12486.

Diabetes - GeneralGlycemic Control

Ketoacidosis in Neonatal Diabetes Mellitus, Part of Wolcott-Rallison Syndrome

Am J Case Rep.

Sreeramaneni PGA, Ambula SRV

Type 1 Diabetes

Case Report: Metreleptin Treatment in a Patient With a Novel Mutation for Familial Partial Lipodystrophy Type 3, Presenting With Uncontrolled Diabetes and Insulin Resistance

Front Endocrinol (Lausanne)

Lambadiari V, Kountouri A, Maratou E, Liatis S, Dimitriadis GD, Karpe F

doi: 10.3389/fendo.2021.684182