Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.

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第一作者： Fakhri,Kallabi

第一单位： Laboratory of Human Molecular Genetics, Faculty of Medicine, Sfax, Tunisia. Electronic address: fakhrikallabi@yahoo.fr.

作者： Fakhri,Kallabi ^[1] ; Neila,Belghuith ^[2] ; Hajer,Aloulou ^[3] ; Thouraya,Kammoun ^[3] ; Soufiane,Ghorbel ^[4] ; Mouna,Hajji ^[5] ; Syrine,Gallas ^[6] ; Jaleleddine,Chemli ^[7] ; Imen,Chabchoub ^[3] ; Hatem,Azzouz ^[8] ; Amel,Ben Chehida ^[8] ; Lamia,Sfaihi ^[3] ; Saloua,Makni ^[5] ; Ali,Amouri ^[9] ; Leila,Keskes ^[10] ; Neji,Tebib ^[8] ; Saayda,Ben Becher ^[5] ; Monjia,Hachicha ^[3] ; Hassen,Kamoun ^[11]

作者单位： Laboratory of Human Molecular Genetics, Faculty of Medicine, Sfax, Tunisia. Electronic address: fakhrikallabi@yahoo.fr. ^[1] Department of Medical Genetics, C.H.U. Hedi Chaker, Sfax, Tunisia. ^[2] Department of Pediatrics, C.H.U. Hedi Chaker, Sfax, Tunisia. ^[3] Department of Pediatric Surgery B, Children's Hospital Bechir Hamza, Tunis, Tunisia. ^[4] Department of Pediatrics, Children's Hospital Bechir Hamza, Tunis, Tunisia. ^[5] Physiology Laboratory, Faculty of Medicine, Monastir, Tunisia. ^[6] Department of Pediatrics, Sahloul Hospital, Sousse, Tunisia. ^[7] Department of Pediatrics, La Rabta Hospital, Tunis, Tunisia. ^[8] Department of Gastroenterology, C.H.U. Hedi Chaker, Sfax, Tunisia. ^[9] Laboratory of Human Molecular Genetics, Faculty of Medicine, Sfax, Tunisia. ^[10] Laboratory of Human Molecular Genetics, Faculty of Medicine, Sfax, Tunisia; Department of Pediatrics, C.H.U. Hedi Chaker, Sfax, Tunisia. ^[11]

关键词 AAAS gene Achalasia Adrenal insufficiency Alacrima Allgrove syndrome Major mutation