Clinical_Rounds_in_Endocrinology_Volume_II_-_Pediatric_Endocrinology
324 How to differentiate between PAIS , 5 α - reductase type 2 defi ciency , and 17β - HSD3 defi ciency? In a patient with bil ...
325 Parameters PAIS 5 α-reductase type 2 17 β-HSD3 defi ciency Prostate Normal/hypoplastic Hypoplastic Normal/hypoplastic Gyneco ...
326 action on Sertoli cell, thereby resulting in decreased production of inhibin B. Therefore, genetic analysis is required for ...
327 Does the presence of gynecomastia help in the differential diagnosis of 46 , XY DSD with genital ambiguity? In patients wi ...
328 converted to androstenedione (and 16α-hydroxy androstenedione) by the pla- cental enzyme 3β-HSD1, which is aromatized to est ...
329 Fig. 9.19 ( a – d ) A 32-year-old well-virilized male presented with primary infertility and karyotype confi rmed 46,XX male ...
330 What is XX male syndrome? 46,XX male syndrome is a DSD characterized by unambiguous male pheno- type with 46,XX karyotype, ...
331 How to assess the psychosexual development of an individual? Psychosexual development (“behavioural sex”) of an individual ...
332 a b Fig. 9.20 ( a ) An individual with OT-DSD reared as male. ( b ) External genitalia showing Tanner pubic hair stage P 3 , ...
333 When should surgery for hypospadias be performed in a child with 46 , XY DSD? In a child with 46,XY DSD and hypospadias, c ...
334 When to consider gonadectomy in a patient with DSD? Decision to perform gonadectomy in a patient with DSDs is based on the ...
© Springer India 2016 335 A. Bhansali et al., Clinical Rounds in Endocrinology, DOI 10.1007/978-81-322-2815-8_10 1 0 Congenital ...
336 fl udrocortisone (100 μg/day) was continued. The annual follow-up of the patient with clinical and biochemical parameters is ...
337 dexamethasone 0.25 mg/day and fludrocortisone 150 μg/day, and with this therapy, 17(OH)P decreased to 40 ng/ml. Hydrocortiso ...
338 passage of maternal progesterone which exerts partial mineralocorticoid agonistic activity in the presence of aldosterone de ...
339 optimal treatment often subsequently results in induction of GDPP. This happens because rapid reduction of androgens with op ...
340 What are the enzymes common for adrenal and gonadal steroidogenesis? The enzymes which are common for adrenal and gonadal ...
341 Why is 21α - hydroxylase defi ciency the most common cause of CAH? Humans have two CYP21A genes, a pseudogene (CYP21A1P) a ...
342 CAH, and genetic mutations are usually not required to confi rm the diagnosis of CAH. Although, there is a good correlation ...
343 What are the differential diagnoses to be considered in a neonate with salt - wasting crisis? One of the characteristic fe ...
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