Publications by authors named "Muhammad D Jawaid"
This rare case from Pakistan highlights the multifactorial etiology of Sertoli Cell Only Syndrome, emphasizing the importance of early identification and management of contributing factors such as trauma, varicocele, and surgical interventions to improve fertility outcomes.
View Article and Find Full Text PDFRare presentation of huge ectopic ureterocele in an adult female: a case report.
Ann Med Surg (Lond)
November 2024
Article Synopsis
- Ectopic ureteroceles are rare in adults but often found in children, typically discovered during pregnancy ultrasounds or through UTI symptoms.
- A 24-year-old woman faced recurrent UTIs and severe urinary retention due to a large ectopic ureterocele, confirmed through imaging and cystoscopy.
- The minimally invasive treatment led to her full recovery and emphasizes the need to consider ectopic ureteroceles in adult women with frequent urinary issues.
Article Synopsis
- This case report highlights dilated cardiomyopathy as a serious heart complication in autoimmune polyendocrine syndrome type 1 (APS-1), stressing the importance of early detection and teamwork among healthcare providers.
- APS-1, a rare genetic disorder caused by mutations in the AIRE gene, typically presents with symptoms like mucocutaneous candidiasis, adrenal insufficiency, and hypoparathyroidism.
- The reported case involves a 28-year-old male with multiple symptoms confirming APS-1, indicating the necessity for comprehensive care and regular follow-up to enhance patient outcomes.
Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder characterized by extreme immune activation and excessive inflammation. It has been reported in patients with familial cases, immunodeficiencies, malignancies, stem cell transplants, and viral etiologies. This report describes acquired HLH associated with Human herpesvirus-6 (HHV-6) infection in a 76-year-old previously healthy male.
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