Aziza Elouali
Overview
Explore the profile of Aziza Elouali including associated specialties, affiliations and a list of published articles.
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Articles
40
Citations
9
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0
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Recent Articles
1.
Ouerradi N, Njoumi C, Ghannam A, Elouali A, Babakhouya A, Rkain M
Cureus
. 2025 Feb;
17(1):e76934.
PMID: 39906429
Rosaï-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a rare and benign histoproliferative disorder of unknown etiology. It commonly presents with bilateral, painless cervical lymphadenopathy...
2.
Bahari H, Zahiri H, Elouali A, Rkain M, Babakhouya A
Cureus
. 2024 Dec;
16(11):e74007.
PMID: 39703245
Cornelia de Lange syndrome is a genetic disorder that affects multiple systems. It is characterized by growth delays and psychomotor retardation associated with various anomalies, including hirsutism, facial dysmorphism, cardiac...
3.
Boudarbala H, Elouali A, Sara A, Rkain M, Babakhouya A
Cureus
. 2024 Dec;
16(11):e73443.
PMID: 39669869
Introduction Rheumatoid purpura, also referred to as Schönlein-Henoch disease, is a form of systemic vasculitis that is characterized by the presence of IgA deposits within the walls of small vessels....
4.
Elouali A, Elmoqaddem H, Bouhmidi M, Rkain M, Babakhouya A
Cureus
. 2024 Oct;
16(9):e69609.
PMID: 39421125
Pycnodysostosis is a rare autosomal recessive bone disorder caused by mutations in the cathepsin K (CTSK) gene, characterized by increased bone density, short stature, and skeletal fragility. This study reports...
5.
Salhi C, Ghanam A, Elouali A, Babakhouya A, Rkain M, Benajiba N
Rev Prat
. 2024 Oct;
74(7):776-777.
PMID: 39412026
No abstract available.
6.
Ouerradi N, Ayad G, Elouali A, Babakhouya A, Rkain M
Cureus
. 2024 Sep;
16(8):e68133.
PMID: 39347221
Congenital Factor VII (FVII) deficiency is a rare autosomal recessive disorder with a prevalence of approximately 1:500,000. It plays a crucial role in initiating coagulation by activating Factors IX and...
7.
Benchaib N, Elouali A, Sara A, Rkain M, Babakhouya A
Cureus
. 2024 Sep;
16(8):e66429.
PMID: 39246904
Sanjad-Sakati syndrome is an autosomal recessive disorder characterized by facial dysmorphia, growth retardation, and congenital hypoparathyroidism. Epidemiologically, this syndrome is primarily observed in children of Arabian descent. However, cases have...
8.
Bouhafs N, Hamami A, Elouali A, Babakhouya A, Rkain M
Cureus
. 2024 Sep;
16(8):e66060.
PMID: 39224741
Portal cavernoma is a major cause of extrahepatic portal hypertension (EHPH) in children. It is a serious condition, due to the frequency and severity of digestive hemorrhages secondary to the...
9.
El Haddadi H, Hamami A, Sara A, Elouali A, Ghanam A, Babakhouya A, et al.
Cureus
. 2024 Aug;
16(7):e64798.
PMID: 39156408
Background: Varicella is a very common childhood infectious disease. It is generally benign, but it can lead to fatal complications. Our study aimed to describe the clinical and therapeutic profile...
10.
Bebana A, Ghanam A, Tkak H, Elouali A, Babakhouya A, Rkain M
Cureus
. 2024 Aug;
16(7):e64595.
PMID: 39149652
Ataxia-telangiectasia (A-T) is a rare inherited autosomal recessive disease. It is associated with an alteration in the gene, located on chromosome 11q22-23, which codes for a protein involved in a...