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eFigure 20–15. Typical basal body temperature and plasma hormone concentrations (mean ± standard error) during a normal 28-day human menstrual cycle. Values are aligned with respect to the day of the midcycle LH peak. FSH, follicle-stimulating hormone, M, menses. (Reproduced with permission from Barrett KE. Ganong's Review of Medical Physiology. 26th ed. McGraw-Hill, 2019.) Four graphs depict the basal body temperature and plasma hormone concentrations during the midcycle L H peak.

Current Medical Diagnosis & Treatment 2025 > Contraception & Family Planning

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eFigure 28–16. Radiographs of index finger of a patient before (left) and after (right) plasma phosphate was reduced to normal with aluminum hydroxide gel and 6 months of dialysis against a bath of 8 mg/dL calcium. (Reproduced, with permission, from Vosik WM et al. Successful medical management of osteitis fibrosa due to tertiary hyperparathyroidism. Mayo Clin Proc. 1972:47:110.) Two radiographs show a patient's index finger before and after dialysis.

Current Medical Diagnosis & Treatment 2025 > Hyperparathyroidism

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eFigure 28–23. Boy, 15-years-old with Kallmann syndrome. His testes were originally undescended, but they descended into the scrotum after human chorionic gonadotropin treatment was given. His height was 163.9 cm (–1.5 SD), and the US:LS ratio was 0.86 (eunuchoid). The penis was 6.3 × 1.8 cm. Each testis was 1 × 2 cm. Plasma LH was not detectable and rose to 5.5 mIU/mL (0.7 ng/mL) after administration of 100 mg of gonadotropin-releasing hormone; FSH rose from 3.6 to 7.2 mIU/mL (1.2–2.4 ng/mL). Testosterone did not change from 17 ng/dL. He had no ability to smell standard odors. (Reproduced, with permission, from Styne DM, Grumbach MM. Reproductive Endocrinology. Yen SSC, Jaffe RB [editors]. Saunders, 1978.) A photo shows a teenage boy, approximately 165 centimeters tall with small penis and absence of pubic hair. A photo shows side view of a teenage boy, approximately 165 centimeters tall.

Current Medical Diagnosis & Treatment 2025 > Male Hypogonadism

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eFigure 28–23. Boy, 15-years-old with Kallmann syndrome. His testes were originally undescended, but they descended into the scrotum after human chorionic gonadotropin treatment was given. His height was 163.9 cm (–1.5 SD), and the US:LS ratio was 0.86 (eunuchoid). The penis was 6.3 × 1.8 cm. Each testis was 1 × 2 cm. Plasma LH was not detectable and rose to 5.5 mIU/mL (0.7 ng/mL) after administration of 100 mg of gonadotropin-releasing hormone; FSH rose from 3.6 to 7.2 mIU/mL (1.2–2.4 ng/mL). Testosterone did not change from 17 ng/dL. He had no ability to smell standard odors. (Reproduced, with permission, from Styne DM, Grumbach MM. Reproductive Endocrinology. Yen SSC, Jaffe RB [editors]. Saunders, 1978.) A photo shows a teenage boy, approximately 165 centimeters tall with small penis and absence of pubic hair. A photo shows side view of a teenage boy, approximately 165 centimeters tall.

Current Medical Diagnosis & Treatment 2025 > Male Hypogonadism

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eFigure 42–8. Hereditary hemorrhagic telangiectasias: Note that the telangiectasias have been treated with argon plasma photocoagulation. (Used with permission from Michelle Nazareth, MD.) An image shows a thin whitish layer covering the blood spots in the stomach lining of a patient.

Current Medical Diagnosis & Treatment 2025 > Hereditary Hemorrhagic Telangiectasia

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