A5041652946- Diet and metabolism studies
- RNA modifications and cancer
- Protein Tyrosine Phosphatases
- Cardiac, Anesthesia and Surgical Outcomes
- Cerebrovascular and Carotid Artery Diseases
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Metabolism and Genetic Disorders
- Cardiac Valve Diseases and Treatments
- Gastrointestinal motility and disorders
- Lipoproteins and Cardiovascular Health
- Migraine and Headache Studies
- Nutrition and Health in Aging
- Sexual Differentiation and Disorders
- Oral and Craniofacial Lesions
- Thyroid and Parathyroid Surgery
- Nutritional Studies and Diet
- Neurological disorders and treatments
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Sympathectomy and Hyperhidrosis Treatments
- Cardiac Imaging and Diagnostics
- Infant Health and Development
- Infective Endocarditis Diagnosis and Management
- Urological Disorders and Treatments
- Frailty in Older Adults
- Intracranial Aneurysms: Treatment and Complications
Nanjing Medical University
2023-2024
Saidu Teaching Hospital
2024
Rutgers, The State University of New Jersey
2024
Rutgers New Jersey Medical School
2024
Karachi Medical and Dental College
2024
Ollscoil na Gaillimhe – University of Galway
2024
Khyber Teaching Hospital
2024
Mayo Clinic in Arizona
2023
37 Military Hospital
2023
Allama Iqbal Medical College
2023
Noonan syndrome is a genetic, developmental disorder characterized by facial deformities, congenital heart defects, webbed neck, wide space nipples, and growth hormone deficiencies. We report case of 15-year-old female patient who presented to the outpatient department with recurrent puffiness both eyes, easy fatiguability, dyspnea on exertion. The condition was associated bilateral proximal muscular weakness lower limbs positive Gower’s sign. On examination, had hypertelorism, shielded...
Background We aimed to explore the association between Geriatric Nutritional Risk Index (GNRI) and risk of low cognitive functions among older adults in United States (US). Methods Utilizing data from National Health Nutrition Examination Study (NHANES) database, a cross-sectional analysis was conducted. The GNRI served as tool for evaluating nutritional status participants, who were categorized into two groups based on their initial scores: those with scores >98 indicating normal...
Fahr's syndrome a rare neurological condition characterized by an abnormal basal ganglia calcification. The has both genetic and metabolic causes. Here, we describe patient who had secondary to hypoparathyroidism, her calcium level raised after the administration of steroid therapy.We presented case 23-year-old female with seizures. Associated symptoms included headache, vertigo, disturbed sleep, reduced appetite. Her laboratory workup revealed hypocalcemia low parathyroid hormone level,...
Jacobs syndrome and congenital adrenal hyperplasia are separate entities but share common clinical features such as ambiguous genitalia. Further studies needed to conclude the relationship between hyperplasia.
Introduction: Headache disorders have been linked with enhanced atherosclerosis, cortical spreading depression, endovascular dysfunction, vasoconstriction, neurogenic inflammation, hypercoagulability, and cervical artery dissection. We aimed to evaluate the risk of cardiovascular cerebrovascular amongst patients status migrainosus migraine aura. Methods: planned a cross-sectional observational study from nationwide inpatient data 2016-2018. Patients intractable migraine, aura, without aura...
Title PageSubmission Category: Case ReportTitle: Report: Coexistence of Jacob Syndrome, congenital Adrenal Hyperplasia, and Ambiguous Genitalia in a Male Infant.Qaisar Ali Khan1; Faiza Amatul-Hadi, BS2; Amritpal Kooner, MA3; Amber Lee4, Rahma Ahmed5, Adithya Nadella6 Harshawardhan Pande 7 , Yaxel Levin- Carrion 8,Muhammad Afzal9,Moses Alfaro, BSA10
Introduction Noonan syndrome is a multisystem, genetic, developmental disorder occurring with the incidence of 1 case per 1000 to 2500 live births in United -States. The condition occurs either sporadic or autosomal dominant manner and affects both males females equally. [1] Ullrich (1930) Turner (1938) described short stature, sexual infantilism, pattern characteristic minor anomalies like pterygium colli. This originally named Ullrich-Turner was later called syndrome. It first reported by...