3 results
21hydroxylasedeficiency anomalous cardiology endocrinology management praderwilli pulmonary return summary syndrome tapvr total venous
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... delayed puberty -> Infertility ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... PVO Present • Diagnosis ... Classic “snowman sign ... #management #cardiology ... #peds #pediatrics
No results found for "infertility pediatrics diagnosis signs radiology sign pathophysiology ct msk peds 21ohd genetics"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #infertility #pediatrics #diagnosis #signs #radiology #sign #pathophysiology #ct #msk #peds #21ohd #genetics