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34 Possible Causes for Gigantism, Hypergonadotrophic Hypogonadism

  • Klinefelter Syndrome

    Hormonal assay revealed hypergonadotrophic hypogonadism on the basis of decreased serum total testosterone ([] Klinefelter syndrome (KS; 47, XXY) is characterized by increased body height, hypergonadotrophic hypogonadism, and infertility.[] Although the phenotype is very variable, features include testicular dysgenesis, elevated gonadotrophins, microorchidism (hypergonadotrophic hypogonadism, and gynacomastia[]

  • Acromegaly

    Growth hormone overproduction Hypersomatotropic gigantism Overproduction of growth hormone Pituitary gigantism Sotos syndrome Sotos' syndrome Applies To Overproduction of[] Hormonal assay revealed hypergonadotrophic hypogonadism on the basis of decreased serum total testosterone ([] Male predominance was seen among AIP -mutated gigantism, whereas X-LAG had a strong female predilection. [5] Signs and symptoms Gigantism The presentation of patients with[]

  • XYY Syndrome

    There are usually no known hormonal deficits among men with 47,XYY, while men with KS often receive testosterone substitution therapy due to hypergonadotrophic hypogonadism[]

  • Hypogonadism

    Alternative names for male hypogonadism Testosterone deficiency syndrome; testosterone deficiency; primary hypogonadism; secondary hypogonadism; hypergonadotrophic hypogonadism[] […] directly to: 2015/16 ICD-10-CM E29.1 Testicular hypofunction Approximate Synonyms Acquired testicular failure Deficiency of testosterone biosynthesis Eunuchism Eunuchoid gigantism[] Primary hypogonadism is also referred to as hypergonadotrophic hypogonadism, whereby the pituitary produces too much luteinising hormone (LH) and follicle stimulating hormone[]

  • Chudley-Rozdilsky Syndrome

    Hypogonadism).[] […] opalescent teeth phosphaturia Cerebral cavernous malformation Cerebral dysgenesis neuropathy ichthyosis and palmoplantar keratoderma syndrome Cerebral folate deficiency Cerebral gigantism[] […] calcifications opalescent teeth phosphaturia * Cerebral cavernous hemangioma * Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome * Cerebral gigantism[]

  • Woodhouse Sakati Syndrome

    hypogonadism with ovaries not visualized on pelvic ultrasound and diabetes mellitus diagnosed at 19 years of age.[] […] deficiency ) - General ( Hypogonadism, Delayed puberty, Precocious puberty ) Other Androgen insensitivity syndrome - Autoimmune polyendocrine syndrome - Carcinoid syndrome - Gigantism[] Hypergonadism Precocious puberty Hypoandrogenism Hypoestrogenism Hyperandrogenism Hyperestrogenism Height Dwarfism / Short stature Midget Laron syndrome Psychosocial Ateliosis Gigantism[]

  • Nivelon-Nivelon-Mabille Syndrome

    hypogonadism) in association with severe dwarfism with generalized chondrodysplasia (bell-shaped thorax, micromelia, brachydactyly).[] […] paraplegia Macrodactyly of the foot Macrodactyly of the hand Macroepiphyseal dysplasia Mcalister Coe type Macroglobulinemia Macroglossia dominant Macroglossia exomphalos gigantism[] […] characterized by the clinical features of 46,XY complete gonadal dysgenesis (see this term; normal external female genitalia, lack of pubertal development, primary amenorrhea, and hypergonadotrophic[]

  • Hypogonadotropic Hypogonadism 22

    Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: D-CHRAMPS syndrome.[] Arthropathy associated with acromegaly ( M14.5* ) Overproduction of growth hormone Excludes: constitutional: · gigantism ( E34.4 ) · tall stature ( E34.4 ) increased secretion[] E21.4 Other specified disorders of parathyroid gland E21.5 Disorder of parathyroid gland, unspecified E22 Hyperfunction of pituitary gland E22.0 Acromegaly and pituitary gigantism[]

  • Turner Syndrome

    Due to hypergonadotrophic hypogonadism, she was proposed an in vitro fertilization (IVF) program with an oocyte donor from unrelated anonymous women.[] To the best of our knowledge, this is the first reported case of simultaneous presence of Turner syndrome and gigantism in the literature.[] The major clinical feature of gigantism is growth acceleration, although these patients also suffer from hypogonadism and soft tissue hypertrophy.[]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    Other characteristics of MSS involve short stature, hypergonadotrophic hypogonadism, and skeletal deformities due to muscle weakness.[] . , Gigante, M., Mascarin, M. , Italia, F., Barresi, L., Barzan, L., Bertola, G. , Buonadonna, A. , Canzonieri, V. & De Paoli, A. , Jan 1 2019 , (Accepted/In press) In : Cancer[] Skre J, Bassöe HH, Berg K, Frövig AG (1976) Cerebellar ataxia and hypergonadotrophic hypogonadism in two kindreds. Chance concurrence, pleiotropism or linkage.[]

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