Výsledky vyhledávání - "Dhoha, Ben salah"

Akademický článek

Neurological Characteristics of Allgrove Syndrome: A Case Series

Autor: Dhoha Ben Salah, Mouna Elleuch, Oumeyma Trimeche, Asma Zargni, Fakhri Kallabi, Salma Sakka, Fatma Mnif, Nabila Rekik, Nadia Charfi, Hassen Kamoun, Mouna Mnif Feki, Faten Hadj Kacem, Mohamed Abid

Publikováno v: Annals of Child Neurology, Vol 32, Iss 2, Pp 130-134 (2024)

Purpose Allgrove syndrome, also known as “triple A” syndrome, is characterized by adrenal insufficiency, achalasia, and alacrimia. When neurological signs are also present, the condition is referred to as “4 A” syndrome. Methods We conducted

Externí odkaz: https://doaj.org/article/047022b12fb7477588ee364b1bf1b2b8

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Akademický článek

Diagnosis and management of pituitary apoplexy: a Tunisian data

Autor: Faten Hadj Kacem, Oumeyma Trimeche, Imen Gargouri, Dhoha Ben Salah, Nadia Charfi, Nabila Rekik, Fatma Mnif, Mouna Mnif, Mouna Elleuch, Mohammed Abid

Publikováno v: Chinese Neurosurgical Journal, Vol 9, Iss 1, Pp 1-7 (2023)

Abstract Background Pituitary apoplexy (PA) is defined as the hemorrhage or the infraction of a pituitary adenoma. Aiming to determine the epidemiological, clinical, paraclinical characteristics as well as management and outcomes of PA in our populat

Externí odkaz: https://doaj.org/article/9027a38e022145f2be46b788ff1250d0

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Akademický článek

Insulinoma with equivocal imaging Wafa

Autor: Wafa Belabed, Fatma Mnif, Abdel Mouhaymen Missaoui, Mouna Elleuch, Dhoha Ben Salah, Nadia Charfi, Mouna Mnif, Nabila Rekik, Faten Hadj Kacem, Mohamed Abid

Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2023)

A 55-year-old patient was admitted to our department for the management of a repetitive alteration of consciousness. Biological investigation results were consistent with endogenous hyperinsulinemic hypoglycemia. Insulinoma was therefore suspected. A

Externí odkaz: https://doaj.org/article/c71dca440e6849f2b2136ea81abfcaae

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Akademický článek

Case report: Management challenges of late diagnosed 17‐alpha hydroxylase deficiency

Autor: Dhoha Ben Salah, Oumeyma Trimeche, Mouna Elleuch, Wafa El abed, Ameni Salah, Fatma Abdelhadi, Hassen Kammoun, Wiem Feki, Zeineb Mnif, Khansa Chaabouni, Fatma Ayedi, Fatma Mnif, Nabila Rekik, Mouna Mnif, Nadia Charfi, Faten Hadj kacem, Mohamed Abid

Publikováno v: Clinical Case Reports, Vol 11, Iss 2, Pp n/a-n/a (2023)

Abstract Herein we report the intriguing case of a 42‐year‐old woman presenting with grade three hypertension, severe hypokalemia and primary amenorrhea, which revealed to be the complete form of 17 alphahydroxylase deficiency. We also discuss th

Externí odkaz: https://doaj.org/article/fa3765463d944ba885cd3dc7abe94aed

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