Persistent Müllerian duct syndrome: A novel mutation in the Αnti-Müllerian Ηormone gene

Ayça Altincik, Fahri Karaca, Hüseyin Onay

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BACKGROUND AND OBJECTIVE: Persistent Müllerian duct syndrome (PMDS) is a relatively rare form of 46,XY disorder of sex development caused by the failure of formation, release or action of anti-Müllerian hormone (AMH) in intrauterine life. In this report we describe a case diagnosed with PMDS with a novel homozygous mutation in the AMH gene …

Congenital nephrogenic diabetes insipidus in the Corpus Hippocraticum: The first description

Gregory Tsoucalas, Marianna Karamanou

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Dear Editor, In congenital nephrogenic diabetes insipidus (cNDI), polyuria and polydipsia are present from birth, as the kidney is unable to concentrate urine despite elevated concentrations of the antidiuretic hormone arginine-vasopressin. In ancient Greek medicine, physiology was, needless, to say, an as yet fairly undeveloped specialty among medico-philosophers …

Melampus and the cure of Proetus’ daughters

Vasiliki Vasileiou, Georgios K. Markantes, Anastasia K. Armeni, Konstantina Barouti, Angeliki Georgopoulou, Neoklis A. Georgopoulos

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Dear Editor, In Greek mythology, Melampus, son of Amythaon was a seer and healer. His name means “black foot” or “man with the black feet” as, according to the legend, when he was a neonate he was left by his mother with his feet exposed to the bright sun. Being the Greek prototype of the shaman, he was, according to Herodotus, the introducer of the worship of Dionysus and the creator of an entire school of magic …