The Experts below are selected from a list of 6 Experts worldwide ranked by ideXlab platform

Swapnil Sharma - One of the best experts on this subject based on the ideXlab platform.

  • Chiari Frommel Syndrome - AN EXHAUSTIVE REVIEW Review Article
    2012
    Co-Authors: Juhi Rao, Neha Sharma, Ekta Singh, Rajani Chauhan, Swapnil Sharma
    Abstract:

    A rare endocrine disorder, an orphan disease, described by a German surgeon, Chiari Johann Baptist, and Frommel Richard Julius Ernst, a German gynecologist is ChiariFrommel Syndrome. It affects the women (usually young, 17‐35 years) who have recently given birth, suffer from galactorrhea, anovulation, and amenorrhea, continuing for an abnormal period of time, uterus atrophy, and is better known as ChiariFrommel Syndrome in which hyperprolactinemia, eosinophillic hyperfunction is observed. But still its physiopathology remains unclear. The main targets of the disorder are those who are poorly nourished and complaint of lactation, lassitude, headaches, abdominal discomfort, mental distress, depression, breast enlargement, decreased size of uterus and cervix, weight gain, fatigue. Different findings reported are lot of variation but usually normal 17 ketosteroid excretion, atrophied endometrium, hypoestrogenic vaginal mucosa, normal glucose and insulin tolerance test, normal basal temperature curve. Related medications are cortef, eulexin, biperiden. Other drugs tried are tri‐p‐anisyl chloroethylene (TACE) with methyl testosterone, levodopa, bromoergocryptine, gamma amino butyric acid. Case reports have been also mentioned in the review.

Juhi Rao - One of the best experts on this subject based on the ideXlab platform.

  • Chiari Frommel Syndrome - AN EXHAUSTIVE REVIEW Review Article
    2012
    Co-Authors: Juhi Rao, Neha Sharma, Ekta Singh, Rajani Chauhan, Swapnil Sharma
    Abstract:

    A rare endocrine disorder, an orphan disease, described by a German surgeon, Chiari Johann Baptist, and Frommel Richard Julius Ernst, a German gynecologist is ChiariFrommel Syndrome. It affects the women (usually young, 17‐35 years) who have recently given birth, suffer from galactorrhea, anovulation, and amenorrhea, continuing for an abnormal period of time, uterus atrophy, and is better known as ChiariFrommel Syndrome in which hyperprolactinemia, eosinophillic hyperfunction is observed. But still its physiopathology remains unclear. The main targets of the disorder are those who are poorly nourished and complaint of lactation, lassitude, headaches, abdominal discomfort, mental distress, depression, breast enlargement, decreased size of uterus and cervix, weight gain, fatigue. Different findings reported are lot of variation but usually normal 17 ketosteroid excretion, atrophied endometrium, hypoestrogenic vaginal mucosa, normal glucose and insulin tolerance test, normal basal temperature curve. Related medications are cortef, eulexin, biperiden. Other drugs tried are tri‐p‐anisyl chloroethylene (TACE) with methyl testosterone, levodopa, bromoergocryptine, gamma amino butyric acid. Case reports have been also mentioned in the review.

Swedish Medical Center Seattle And Issaquah - One of the best experts on this subject based on the ideXlab platform.

  • Walsh & Hoyt: Sarcoidosis: Endocrine Manifestations
    Spencer S. Eccles Health Sciences Library University of Utah, 2005
    Co-Authors: Steven R. Hamilton, Swedish Medical Center Seattle And Issaquah
    Abstract:

    A variety of endocrine disorders can develop in patients with sarcoidosis. As already discussed, disturbed calcium metabolism can lead to hypercalcemia, hypercalciuria, and decreased fecal excretion of calcium. Sarcoidosis that affects the hypothalamus can produce clinical manifestations of hypothalamic and pituitary dysfunction, including partial or panhypopituitarism, diabetes insipidus, the Chiari-Frommel Syndrome, and the Frolich Syndrome. Hypopituitarism also can result from infiltration of the pituitary gland itself. In addition, sarcoidosis can affect the thyroid gland, parathyroid glands, adrenal glands, and pancreas. In many cases, infiltration of these glands by sarcoid granulomas is an incidental finding detected at autopsy; however, sarcoidosis of specific organs may produce hypothyroidism, hypoparathyroidism, adrenal insufficiency or frank Addison disease, or pancreatitis

Neha Sharma - One of the best experts on this subject based on the ideXlab platform.

  • Chiari Frommel Syndrome - AN EXHAUSTIVE REVIEW Review Article
    2012
    Co-Authors: Juhi Rao, Neha Sharma, Ekta Singh, Rajani Chauhan, Swapnil Sharma
    Abstract:

    A rare endocrine disorder, an orphan disease, described by a German surgeon, Chiari Johann Baptist, and Frommel Richard Julius Ernst, a German gynecologist is ChiariFrommel Syndrome. It affects the women (usually young, 17‐35 years) who have recently given birth, suffer from galactorrhea, anovulation, and amenorrhea, continuing for an abnormal period of time, uterus atrophy, and is better known as ChiariFrommel Syndrome in which hyperprolactinemia, eosinophillic hyperfunction is observed. But still its physiopathology remains unclear. The main targets of the disorder are those who are poorly nourished and complaint of lactation, lassitude, headaches, abdominal discomfort, mental distress, depression, breast enlargement, decreased size of uterus and cervix, weight gain, fatigue. Different findings reported are lot of variation but usually normal 17 ketosteroid excretion, atrophied endometrium, hypoestrogenic vaginal mucosa, normal glucose and insulin tolerance test, normal basal temperature curve. Related medications are cortef, eulexin, biperiden. Other drugs tried are tri‐p‐anisyl chloroethylene (TACE) with methyl testosterone, levodopa, bromoergocryptine, gamma amino butyric acid. Case reports have been also mentioned in the review.

Ekta Singh - One of the best experts on this subject based on the ideXlab platform.

  • Chiari Frommel Syndrome - AN EXHAUSTIVE REVIEW Review Article
    2012
    Co-Authors: Juhi Rao, Neha Sharma, Ekta Singh, Rajani Chauhan, Swapnil Sharma
    Abstract:

    A rare endocrine disorder, an orphan disease, described by a German surgeon, Chiari Johann Baptist, and Frommel Richard Julius Ernst, a German gynecologist is ChiariFrommel Syndrome. It affects the women (usually young, 17‐35 years) who have recently given birth, suffer from galactorrhea, anovulation, and amenorrhea, continuing for an abnormal period of time, uterus atrophy, and is better known as ChiariFrommel Syndrome in which hyperprolactinemia, eosinophillic hyperfunction is observed. But still its physiopathology remains unclear. The main targets of the disorder are those who are poorly nourished and complaint of lactation, lassitude, headaches, abdominal discomfort, mental distress, depression, breast enlargement, decreased size of uterus and cervix, weight gain, fatigue. Different findings reported are lot of variation but usually normal 17 ketosteroid excretion, atrophied endometrium, hypoestrogenic vaginal mucosa, normal glucose and insulin tolerance test, normal basal temperature curve. Related medications are cortef, eulexin, biperiden. Other drugs tried are tri‐p‐anisyl chloroethylene (TACE) with methyl testosterone, levodopa, bromoergocryptine, gamma amino butyric acid. Case reports have been also mentioned in the review.