A5093322292- Lymphadenopathy Diagnosis and Analysis
- Infectious Diseases and Mycology
- Hemoglobinopathies and Related Disorders
- Sexual Differentiation and Disorders
- Neurofibromatosis and Schwannoma Cases
- Dermatology and Skin Diseases
- Vascular Malformations Diagnosis and Treatment
- Meningioma and schwannoma management
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Iron Metabolism and Disorders
- Tumors and Oncological Cases
- Advancements in Transdermal Drug Delivery
- Skin Protection and Aging
- Sperm and Testicular Function
- Blood groups and transfusion
Dow University of Health Sciences
2023-2025
ABSTRACT A class of hereditary diseases known as neurofibromatoses results in tumor growth on tissue from nerves. The spinal cord, nerves, and brain are among the parts nervous framework where these tumors can form. Similar to other genetic disorders, neurofibromatosis discloses complicated phenotypes, exhibiting varying benign malignant skin lesions. Apart symptoms this disease, its origin has also been observed be a challenging task for physician. Tracking signs indicated often leads...
Hemoglobin D variations are a group of hemoglobinopathies caused by mutations in the genes that control synthesis new globin chains. D-Punjab is most prevalent but frequently asymptomatic, it can occasionally cause mild to moderate hemolytic anemia, making diagnosis difficult and raising risk misdiagnosis. This article discusses rare instance seventeen-year-old male Sindh, Pakistan with iron deficiency anemia who was later found have Punjab variation hemoglobin D. The patient had signs...
Kikuchi-Fujimoto disease (KFD) commonly manifests with symptoms of fever, tender cervical adenopathy, and systemic like night sweats, rashes, headache, weight loss, nausea, vomiting, sore throat. In this case study, a 27-year-old patient's main complaints included neck oedema, loss that started one month ago. Following preliminary inquiries, ultrasonography, CT scans, multidisciplinary team has been overseeing the case. After biopsy axillary lymph nodes, it diagnosed as overlapping Systemic...
The urea composition has a profound effect on skin disorders, specifically xerosis, desquamation, and scaling, which are some of the main concerns current health industry. application is relatable more bioactive than alternate treatments. objective this systematic review was to evaluate effectiveness topically applied in treatment ichthyosis, psoriasis, other dermatologic conditions. Research articles were retrieved through electronic databases, including Google Scholar, PubMed, EMBASE,...
Swyer syndrome is a condition where individuals with 46XY karyotype, typically associated males, display complete gonadal dysgenesis and lack testicular differentiation. This results from mutation in the SRY gene, which essential for testis development. As consequence, affected who appear phenotypically female have male chromosomes but do not develop functional testes. result, there an absence of testosterone that leads to masculinization presence genitalia. article describes 20-year-old...