Publications by authors named "Rayan Badawi"
Article Synopsis
- The paper discusses a rare case of a 17-year-old female with deficiencies in coagulation factors VIII (FVIII) and XI (FXI), presenting symptoms of prolonged nosebleeds and heavy menstrual bleeding.
- Despite Hemophilia A and B typically being X-linked disorders, this case highlights how females can still be affected under certain genetic conditions.
- The study emphasizes the importance of considering X-linked Hemophilia as a potential diagnosis in females with unexplained bleeding disorders, alongside more common conditions like Von Willebrand disease.
Background: Scientific research has an essential role in building up the basics of public health and clinical care. As a developing country, Syria has a limited contribution to scientific research. Besides, the current Syrian crisis has inflicted severe damage to the infrastructure of the country, which, in turn, negatively affected the scientific sphere.
View Article and Find Full Text PDFBackground: Fraser syndrome or "cryptophthalmos syndrome" is a rare autosomal recessive disease. It is characterized by a group of congenital malformations such as: crytophthalmos, syndactyly, abnormal genitalia, and malformations of the nose, ears, and larynx. Although cryptophthalmos is considered as a main feature of Fraser syndrome, its absence does not exclude the diagnosis.
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