Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Siham El Haddad PhD"'
Autor:
Eric Michel Charlemagne Junior Kessi MD, Kaoutar Maslouhi MD, Yousra Guelzim MD, Lina Belkouchi PhD, Nazik Allali PhD, Latifa Chat PhD, Siham El Haddad PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
Hemophilia is a congenital coagulopathy characterized by a deficiency of coagulation factors and the development of haematomas and haemarthrosis, either spontaneously or after minor trauma. Recurrent joint hemorrhage in hemophilia patients leads to p
Externí odkaz:
https://doaj.org/article/77bc78c1e07842b69cd513b7303afa07
Autor:
Chaymae Faraj MD, Sara Essetti MD, Kaoutar Maslouhi MD, Nazik Allali PhD, Siham El haddad PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
The arteria lusoria or retroesophageal right subclavian artery is the most common malformation of the aortic arch. It may be discovered with some symptoms of airway and/or esophageal compression, such as dyspnea or dysphagia, but in most cases it is
Externí odkaz:
https://doaj.org/article/74380d4b217f4fdfa58aa8d61bffd65c
Autor:
Ihssane Lahlou PhD, Sara Essetti PhD, Samia Obilat PhD, Fatima Chait PhD, Nourrelhouda Bahlouli PhD, Yousra Guelzim PhD, Siham El Haddad PhD, Nazik Allali PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
Fibrous dysplasia is a rare non-hereditary congenital condition characterized by 2 main forms: monostotic and polyostotic. Monostotic is the more common form, while polyostotic, often associated with a syndrome, is rarer. The case presented involves
Externí odkaz:
https://doaj.org/article/a360ec92028e481ab8dbb203cb98ea0d
Autor:
Fatima Chait MD, Nourrelhouda Bahlouli MD, Khadija Laasri MD, Kaouthar Sfar MD, Najat Lamalmi PhD, Nazik Allali PhD, Siham El Haddad PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
Burkitt’s lymphoma is rare but highly aggressive and very fast-growing B-cell non-Hodgkin’s lymphoma (NHL). It can affect any organ such as the central nervous system, jaw, intestines, kidneys, ovaries, and other organs. It results from the malig
Externí odkaz:
https://doaj.org/article/6ad6899c1d5648e19c987d41e454721a
Autor:
Amine Naggar MD, Saad Assila MD, Khadija Laasri MD, Hajar Andour MD, Zineb Izi MD, Najat Lamalmi PhD, Siham El Haddad PhD, Nazik Allali PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
Nephrogenic rests (NRs) are foci of embryonic nephrogenic cells that persist beyond the 36th week of gestation. They are precursor lesions of Wilms tumor and are found incidentally in approximately 1% of infants. The term nephroblastomatosis (NBS) is
Externí odkaz:
https://doaj.org/article/5fb2e0a0f8de4c62b57fb951123ea890
Autor:
Zakia El Yousfi MD, Ismail Mohamed Halfi MD, Salma El Houss MD, Nazik Allali PhD, Siham El Haddad PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
The superior mesenteric artery syndrome also known as Wilkie’s syndrome or Benign duodenal stasis, is a condition that occurs when the third duodenum is compressed between the superior mesenteric artery anteriorly and the abdominal aorta posteriorl
Externí odkaz:
https://doaj.org/article/b80b585d3de94b788121168eebcfe0cd
Autor:
Badr Kabila MD, Basma Beqqali MD, Samia Obilat MD, Siham El Haddad PhD, Nazik Allali PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
The brown tumor is a non-neoplastic lesion resulting from an abnormality in bone metabolism in the context of primary, secondary, or tertiary hyperparathyroidism. They can affect any bone structure and be single or multiple. They are usually located
Externí odkaz:
https://doaj.org/article/b93321c606644fc8b4bb57890abcdbe0
Autor:
Fatima Chait MD, Nourrelhouda Bahlouli MD, Rachida Chehrastane MD, Nidal Mrani Alaoui PhD, Fadoua Boughaleb MD, El alami Zouheir PhD, El Medhi Tarik PhD, Nazik Allali PhD, Siham El Haddad PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Poland syndrome is indeed a rare congenital malformation that can present with various degrees of thoracic and homolateral upper limb anomalies. The classic features of Poland syndrome include agenesis or hypoplasia of the sternocostal head of the pe
Externí odkaz:
https://doaj.org/article/2b22d75eda854fb18353e5c0e6cb7731
Autor:
Meriem Zhim MD, Khadija Laasri MD, Amine Naggar MD, Soufiane Rostoum MD, Kaoutar Sfar MD, Nazik Allali PhD, Siham El Haddad PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Fetus in fetu is an uncommon medical anomaly characterized by the presence of a malformed fetus within the body of a living twin. Although the retroperitoneum is the most typical location, occurrences in the sacrococcygeal and dorsolumbar regions are
Externí odkaz:
https://doaj.org/article/c2a168a3c7eb429b8c49472c3842bb4c
Autor:
Amine Naggar MD, Hajar Andour MD, Hamza Bensaghir MD, Badr Kabila MD, Chaimae Ben Driss MD, Soukaina El Aouni MD, Monim Ochan PhD, Mounir Kisra PhD, Najat Lamalmi PhD, Siham El Haddad PhD, Nazik Allali PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Mesenchymal hamartoma (MH) is a benign liver tumor accounting for 3% to 8% of all liver tumors in children, commonly manifesting before 3 years of life. Distinguishing MH from hepatoblastoma and other liver tumors relies on imaging and alpha-fetoprot
Externí odkaz:
https://doaj.org/article/a1397d4ede634b2ab4b4471a3de15c0e