Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Amel BEN Hamed"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 12 (2024)
Prune belly syndrome is a rare disorder that occurs mainly in men. It is characterized by the triad of deficient abdominal wall muscles, the dilated urinary collecting system, bilateral cryptorchidism, and infertility. It mainly affects the genitouri
Externí odkaz:
https://doaj.org/article/56d95b166a374b008bdf5bca9b515649
Autor:
Manel Kammoun, Anouar jarraya, Hechem bradai, Hind ketata, Hasna Bouchaira, Olfa Cherif, Amel Ben Hamed, Faiza Safi, Riadh Mhiri
Publikováno v:
Journal of Neonatal Surgery, Vol 13 (2023)
Background: Neonatal surgery in developing countries remains a high-risk modality p and its outcomes depend on various patient-related, system-related, and management-related factors. This study aims to describe our experience in managing newborns re
Externí odkaz:
https://doaj.org/article/12f14fe06b06436e86164e1c89e9a875
Autor:
Anouar Jarraya, Manel Kammoun, Chiraz Regaieg, Khadija Ben Ayed, Abdennaceur Bouattour, Souha Kallel, Fathi Karray, Amel Ben Hamed, Nedia Ben Hamida
Publikováno v:
Journal of Neonatal Surgery, Vol 12 (2023)
Externí odkaz:
https://doaj.org/article/bd524109737845c2bef811a6616cd0f8
Autor:
Nadia Kolsi, Fatma Boudaya, Afef Ben Thabet, Manel Charfi, Chiraz Regaieg, Amira Bouraoui, Ridha Regaieg, Nedia Hentati, Amel Ben Hamed, Abdellatif Gargouri
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Treacher Collins syndrome (TCS) is one of the rare genetic syndromes which is specified by symmetrical craniofacial dysmorphism without growth abnormalities or neurological disorders. The inheritance is usually autosomal dominant but sometim
Externí odkaz:
https://doaj.org/article/96a7fa1144504c9ab5c91a3806340fe5
Autor:
Saloua Ammar, Manar Hbaieb, Mohamed Zouari, Hayet Zitouni, Chiraz Regaieg, Amel BEN Hamed, Mahdi Ben Dhaou, Abdellatif Gargouri, Zeineb Mnif, Riadh Mhiri
Publikováno v:
Journal of Neonatal Surgery, Vol 8, Iss 2 (2019)
Perirenal lymphatic malformation (LM) is a rare benign lesion that often simulate as perinephric collection or parapelvic cyst. A neonate, antenatally diagnosed with a renal cystic mass, was investigated to have a perirenal LM on postnatal ultrasonog
Externí odkaz:
https://doaj.org/article/fe22b82f21bc49deb01089452685be16
Autor:
Chiraz Regaieg, Meriam Triki, Manel Charfi, Slim Charfi, Fathi Karray, Mohamed Abdelmoula, Tahya Boudawara, Amel Ben Hamed, Nedia Hmida
Publikováno v:
Fetal and Pediatric Pathology. :1-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af5fa054cc0ee19cfd86a030815b884f
https://doi.org/10.1080/15513815.2023.2176728
https://doi.org/10.1080/15513815.2023.2176728
Autor:
Abdellatif Gargouri, Mahdi Ben Dhaou, Manar Hbaieb, Mohamed Zouari, Chiraz Regaieg, Riadh Mhiri, Saloua Ammar, Amel Ben Hamed, Zeineb Mnif, Hayet Zitouni
Publikováno v:
Journal of Neonatal Surgery, Vol 8, Iss 2 (2019)
Perirenal lymphatic malformation (LM) is a rare benign lesion that often simulate as perinephric collection or parapelvic cyst. A neonate, antenatally diagnosed with a renal cystic mass, was investigated to have a perirenal LM on postnatal ultrasonog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e4f3429c80d9f4852d07b1914067594
https://jneonatalsurg.com/ojs/index.php/jns/article/view/349
https://jneonatalsurg.com/ojs/index.php/jns/article/view/349
Autor:
Amel Ben Hmed, Abdellatif Gargouri, Manel Charfi, Hassen Kamoun, Chiraz Regaieg, Amira Bouraoui, Nedia Hmida, Afef Ben Thabet, Amel Ben Hamed, Iklas Ben Ayed
Publikováno v:
Abstracts.
Introduction Wolf-Hirschhorn syndrome is a rare condition including a characteristic facial appearance, delayed growth and development, hypotonia, intellectual disability and seizures. Its frequency is estimated at 1/20000 to 1/50000 births with a fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::186d89f7935523ef257798e5625bf23d
https://doi.org/10.1136/archdischild-2019-epa.474
https://doi.org/10.1136/archdischild-2019-epa.474
Autor:
Amira Bouraoui, Chiraz Regaieg, Hamida Turki, Amel Ben Hamed, Afef Ben Thabet, Abderahmen Masmoudi, Nedia Hmida, Manel Charfi, Abdellatif Gargouri, Ridha Regaieg
Publikováno v:
Abstracts.
Background Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital cutaneous vascular anomaly. About 300 cases were reported in the litterature. It is associated persistent cutis marmorata, telangiectasia, and phlebectasia. Case report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4aec394617208aa8195ffd1a0bca076
https://doi.org/10.1136/archdischild-2019-epa.923
https://doi.org/10.1136/archdischild-2019-epa.923
Autor:
Mohamed Derbel, Chiraz Regaieg, Abdellatif Gargouri, Ridha Regaieg, M. Charfi, Samir Kamoun, Mouna Loukil, Nedia Hmida, Amira Bouraoui, Kais Chaabene, Afef Ben Thabet, Dorra Abid, Amel Ben Hamed
Publikováno v:
Abstracts.
Background Neonatal lupus erythematosus (NLE) is an uncommon acquired autoimmune disease caused by transplacental passage of maternal anti-SSA/Ro and anti-SSB/La antibodies. The most common effects of NLE include cutaneous involvement and congenital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc9b9a813d26e4ae17385f139d5d5f7d
https://doi.org/10.1136/archdischild-2019-epa.776
https://doi.org/10.1136/archdischild-2019-epa.776