Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Achraf Chadli, Debbiche"'
Autor:
Khouloud Ben Lazreg, Imen Helal, Fatma Khanchel, Aida Daieb, Sameh Tlili, Sirine El fekih, Ehsen Ben Brahim, Youssef Hellal, Raja Jouini, Achraf Chadli Debbiche
Publikováno v:
Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Splenogonadal fusion is an abnormal connection between the spleen and gonads. This rare entity can be easily confused with testicular tumors. It usually accompanies congenital malformations, such as cryptorchidism, making diagnosis more diff
Externí odkaz:
https://doaj.org/article/76dc57bf7c7540309b88bc8ca9b23887
Autor:
Maissa Ben Thayer, Imen Hlel, Fatma Khanchel, Chaouki Mbarki, Hajer Bettaieb, Ehsen Ben Brahim, Raja Jouini, Achraf Chadli Debbiche
Publikováno v:
Clinical Case Reports. 10
Several hundred cases of placental hemangiomas have been reported in the literature. However, the umbilical cord is extremely uncommon as a site of occurence.We report the first case of hemangioma of the umbilical cord synchronous to maternal infecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::358f6c559fe95435cb0b0ac8a17dafca
https://doi.org/10.1002/ccr3.6441
https://doi.org/10.1002/ccr3.6441
Autor:
Raja, Jouini, Raoueh, Hedhli, Fatma, Khanchel, Mèriem, Sabbah, Dorra, Trad, Imen, Hlel, Wafa, Koubaa, Olfa, Khayat, Ehsen, Ben Brahim, Achraf Chadli, Debbiche
Publikováno v:
La Tunisie medicale. 97(12)
Anguillulosis is a ubiquitous digestive parasitosis. Rare in Tunisia, it is due to a round worm, strongyloid stercoralis, whose natural lodging is the duodeno-jejunal mucosa. Its malignant form is rare but it represents a potentially life-threatening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd49518ecb5e61fe3469679c542a0978
https://pubmed.ncbi.nlm.nih.gov/32173814
https://pubmed.ncbi.nlm.nih.gov/32173814
Autor:
Mourad Mokni, S. Fenniche, Meriem Jones, Khadija Sellami, Anissa Zaouak, Raja Jouini, Hager Jaouadi, Olfa Messaoud, Ridha Mrad, Mariem Chargui, Houda Hammami, Hamida Turki, Sonia Abdelhak, Rym Benkhalifa, Achraf Chadli Debbiche, Karima Chraiet
Publikováno v:
The Journal of dermatology. 45(8)
H syndrome is a rare autosomal recessive disorder with characteristic dermatological findings consisting of hyperpigmentation and hypertrichosis patches mainly located on the inner thighs and multisystemic involvement including hepatosplenomegaly, he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75703ea0620fb2a91cac17d852e7220a
https://pubmed.ncbi.nlm.nih.gov/29808591
https://pubmed.ncbi.nlm.nih.gov/29808591
Autor:
Cherine Charfeddine, Ahlem Sabrine Ben Brick, Samy Fenniche, Rym Benmously, Mourad Mokni, Achraf Chadli Debbiche, Mbarka Bchetnia, Mohamed Ben Ayed, Mohamed Fajraoui, Youssef Ben Ameur, Inçaf Mokhtar, Sonia Abdelhak
Publikováno v:
Archives of dermatological research. 301(8)
Darier's disease (DD, MIM 124200) also known as Darier-White disease and keratosis follicularis, is a rare autosomal dominant skin disorder characterized by warty papules and plaques in the seborrheic area (central trunk, flexures, scalp, and forehea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99de3bfc42a7b1e7b778bfda29d0707b
https://pubmed.ncbi.nlm.nih.gov/19488774
https://pubmed.ncbi.nlm.nih.gov/19488774