• Kallmann syndrome (KS) is a genetic disorder that prevents a person from starting or fully completing puberty. Kallmann syndrome is a form of a group of...
    46 KB (5,150 words) - 17:42, 17 October 2024
  • Thumbnail for Androgen insensitivity syndrome
    limb malformations) Popliteal pterygium syndrome (associated with extensive webbing behind knees) Kallmann syndrome (often associated with anosmia) Hypospadias...
    128 KB (12,638 words) - 22:10, 6 September 2024
  • Thumbnail for Dandy–Walker malformation
    Coffin–Siris syndrome, Meckel–Gruber syndrome type 7 and Kallmann syndrome, among many others. DWM has also been associated with 3C syndrome, Rubinstein–Taybi...
    47 KB (5,483 words) - 15:13, 2 March 2024
  • Thumbnail for ANOS1
    encoded by the ANOS1 gene. Mutations in this gene cause the X-linked Kallmann Syndrome. The encoded protein is similar in sequence to proteins known to function...
    5 KB (644 words) - 12:55, 29 July 2023
  • syndrome Jerusalem syndrome Kabuki syndrome Kallmann syndrome Kapur–Toriello syndrome Karak syndrome Karsch-Neugebauer syndrome Kartagener's syndrome...
    42 KB (4,070 words) - 17:09, 1 October 2024
  • Thumbnail for Fertile eunuch syndrome
    gonadotropins (FSH and LH) Sex hormones (androgens and estrogens) Kallmann syndrome and GnRH insensitivity Valdes-Socin H, Rubio Almanza M, Tomé Fernández-Ladreda...
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  • and dementia with Lewy bodies. Lifelong hyposmia could be caused by Kallmann syndrome or Autism Spectrum Disorder. Along with other chemosensory disturbances...
    7 KB (806 words) - 14:46, 27 November 2022
  • tumor caused by Human herpesvirus 8 (HHV8) Kartagener syndrome, a genetic disorder Kallmann syndrome, a genetic disorder preventing the start or completion...
    3 KB (385 words) - 19:23, 4 September 2024
  • Thumbnail for Aureliano Maestre de San Juan
    known as Kallmann syndrome. He died in 1890, having been blinded in a laboratory accident involving caustic soda two years earlier. Kallmann syndrome Maestre...
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    had a smaller thalamus. A loss of function mutation in FEZF1 causes Kallmann Syndrome. As axons are developing and migrating in the early embryo, FEZF1...
    4 KB (611 words) - 19:29, 13 April 2022
  • Delayed puberty (category CS1 German-language sources (de))
    Puberty Constitutional growth delay Hypogonadism Kallmann syndrome Turner syndrome Klinefelter syndrome Hoffman B (2016). Williams Gynecology. McGraw-Hill...
    44 KB (4,972 words) - 22:14, 6 September 2024
  • dysphalangism syndrome Brachyolmia recessive Hobaek type Brachyolmia Brachytelephalangy characteristic facies Kallmann Braddock–Carey syndrome Braddock–Jones–Superneau...
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  • municipality of Concepcion, Romblon in the Philippines Maestre-Kallmann-Morsier syndrome, a genetic disorder Maestro Master (disambiguation) This page...
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  • Thumbnail for Olfactory tract
    ability to smell). Anosmia either total or partial is a symptom of Kallmann syndrome a genetic disorder that results in disruption of the development of...
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  • Thumbnail for Female infertility
    causing female infertility include Turner syndrome. Oocyte donation is an alternative for patients with Turner syndrome. Some of these gene or chromosome abnormalities...
    63 KB (7,112 words) - 11:14, 23 July 2024
  • sex determining region Y-Box 10 (SOX10), GNRHR, GNRH1 and KISS1R. Kallmann syndrome results in a loss of smell (anosmia) and is associated with KAL1 mutations...
    14 KB (1,754 words) - 17:31, 11 September 2024
  • 14 in females and 15 in males is Kallmann syndrome, a form of hypogonadotropic hypogonadism (HH). Kallmann syndrome is also associated with a lack of...
    92 KB (10,876 words) - 05:46, 27 August 2024
  • Jones–Smith Syndrome – Kenneth Lyons Jones, David Weyhe Smith Kahler's disease – Otto Kahler Kallmann syndrome – Franz Josef Kallmann Kanner syndrome – Leo...
    63 KB (6,564 words) - 19:18, 15 October 2024
  • Thumbnail for Prokineticin receptor 2
    then triggers calcium release inside the cell. Prokineticin receptor Kallmann syndrome GRCh38: Ensembl release 89: ENSG00000101292 – Ensembl, May 2017 GRCm38:...
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  • Thumbnail for Hypopituitarism
    deficiency is associated with obesity, raised cholesterol and the metabolic syndrome, and estradiol deficiency may lead to osteoporosis. While effective treatment...
    41 KB (4,441 words) - 21:58, 6 September 2024
  • Thumbnail for Osteoporosis
    cause secondary osteoporosis. These include Turner syndrome, Klinefelter syndrome, Kallmann syndrome, anorexia nervosa, andropause, hypothalamic amenorrhea...
    124 KB (13,987 words) - 18:32, 4 October 2024
  • Thumbnail for Intersex
    conditions such as late onset congenital adrenal hyperplasia and Klinefelter syndrome, which most clinicians do not recognize as intersex; Sax states, "if the...
    156 KB (14,658 words) - 06:30, 29 September 2024
  • Thumbnail for Boston City Hall
    designed by Gerhard Kallmann, a Columbia University professor, and Michael McKinnell, a Columbia graduate student who co-founded Kallmann McKinnell & Knowles...
    44 KB (4,593 words) - 22:37, 22 August 2024
  • Thumbnail for Azoospermia
    azoospermia may be caused by congential hypopituitarism, Kallmann syndrome, Prader-Willi syndrome and other genetic conditions that lead to GnRH or gonadotropin...
    23 KB (2,531 words) - 05:29, 15 August 2024
  • Thumbnail for CHD7
    mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome". Clinical Genetics. 75 (1): 65–71. doi:10.1111/j...
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  • Thumbnail for GnRH neuron
    cause reproductive disorders like hypogonadotropic hypogonadism or Kallmann Syndrome. In 1989, two research groups independently discovered that GnRH neurons...
    11 KB (1,353 words) - 08:56, 2 July 2024
  • Thumbnail for Luteinizing hormone
    observed. Conditions with very low LH secretions include: Pasqualini syndrome Kallmann syndrome Hypothalamic suppression Hypopituitarism Eating disorder Female...
    34 KB (3,380 words) - 00:57, 12 October 2024
  • Thumbnail for Gonadotropin-releasing hormone
    activity, as seen in polycystic ovary syndrome (PCOS). GnRH formation is congenitally absent in Kallmann syndrome. At the pituitary, GnRH stimulates the...
    27 KB (3,150 words) - 08:47, 11 April 2024
  • that does not subsequently progress. Of note, the X-linked form of Kallmann syndrome (KS) form of GnRH insensitivity relating to mutations in the ANOS1...
    23 KB (2,665 words) - 14:49, 12 October 2024
  • 1418–28. doi:10.1016/s0006-3223(99)00231-0. PMID 10578456. S2CID 45154449. Kallmann FJ, Roth B (February 1956). "Genetic aspects of preadolescent schizophrenia"...
    49 KB (5,997 words) - 19:58, 18 September 2024