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17 Possible Causes for Kallmann Syndrome, Male Infertility due to Globozoospermia

  • Kallmann Syndrome

    Kallmann syndrome is the result of a genetic defect.[symptoma.com] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] It is not clear if the malformation is in association with Kallmann syndrome or purely coincidental.[ncbi.nlm.nih.gov]

  • Cryptorchidism

    Whereas the duplication mutation has not been reported before, p.Pro26Leu was once observed in a Kallmann syndrome patient.[ncbi.nlm.nih.gov] syndrome cystic fibrosis testicular feminization Prognosis, Prevention, and Complications Prognosis most descend by 3 months if natural descent does not occur by this time[step1.medbullets.com] Meningomyelocele Hypospadias Wilms tumor Prader-Willi syndrome Kallmann syndrome Cystic fibrosis -- To view the remaining sections of this topic, please sign in or purchase[unboundmedicine.com]

  • Klinefelter Syndrome

    All patients with Kallmann syndrome required long term testosterone treatment.[ncbi.nlm.nih.gov] Keywords Intelligence Quotient Gynecomastia Klinefelter Syndrome Kallmann Syndrome Performance Intelligence Quotient Disease name and synonyms Klinefelter syndrome (KS) –[doi.org] Postpubertal males with Klinefelter syndrome (n 32) and Kallmann syndrome (n 19) were audited by chart review for psychosocial comorbidities, pubertal management, and the[ncbi.nlm.nih.gov]

  • Male Infertility due to Globozoospermia

    Other genetic syndromes associated with infertility include cystic fibrosis, Kallmann's syndrome and Kartagener's syndrome. Problems with sexual intercourse.[mayoclinic.org] CONCLUSION(S): ICSI is an effective treatment in couples that failed to conceive spontaneously within 1 year combined with male infertility due to partial globozoospermia.[ncbi.nlm.nih.gov] The congenital form, known also as Kallmann's syndrome, is caused by lower amounts of gonadotropin-releasing hormone (GnRH). GnRH is a hormone made by the hypothalamus.[urologyhealth.org]

  • Hyperthyroidism

    Kallmann syndrome (KS) is a clinically and genetically heterogeneous disorder characterized by hypogonadotropic hypogonadism and olfactory dysfunction.[ncbi.nlm.nih.gov]

  • Oligospermia

    Other genetic syndromes associated with infertility include cystic fibrosis, Kallmann's syndrome and Kartagener's syndrome. Celiac disease.[mayoclinic.org] In addition, Kallmann's syndrome also is associated with anosmia, a lack of sense of smell, which should be evaluated during the physical examination.[glowm.com] Kallmann syndrome is due to a congenital lack of GnRH secretion.[gfmer.ch]

  • Sertoli Cell-Only Syndrome

    ’s syndrome Klinefelter syndrome Sertoli-cell only syndrome Klinefelter syndrome and Sertoli-cell only syndrome have no known medical treatment unless sperm can be identified[rscbayarea.com] It is commonly seen with Kallmann syndrome, androgen resistance, and defects in testosterone synthesis.[omicsonline.org] […] can impact either the production or delivery of healthy sperm: Congenital absence of the vas deferens (CAVD) Undescended testes, also known as cryptorchidism Hypospadias Kallmann’s[rscbayarea.com]

  • Bloom Syndrome

    ジュベー症候群 MarieJoubert Canadian neurologist Kahn カーン Kahn test カーンテスト Kallmann カルマン Kallmann syndrome カルマン症候群 Kaposi カポジ Kaposi's sarcoma カポジ肉腫 Móric Kaposi (1837 -1902) Hungarian[jams.med.or.jp] Jeune syndrome ジューヌ症候群 Johne ヨーネ Johne's disease ヨーネ病 Jolly ジョリー Jolly reaction ジョリー反応 Jones-Mote ジョーンズ・モート Jones-Mote hypersensitivity ジョーンズ・モート過敏症 Joubert ジュベー Joubert syndrome[jams.med.or.jp]

  • Myotonic Dystrophy

    ) FGFR1 ( Pfeiffer syndrome, KAL2 Kallmann syndrome ) FGFR2 ( Apert syndrome, Antley–Bixler syndrome, Pfeiffer syndrome, Crouzon syndrome, Jackson–Weiss syndrome ) FGFR3[en.wikipedia.org] CASR ( Familial hypocalciuric hypercalcemia ) Class F FZD4 ( Familial exudative vitreoretinopathy 1 ) Enzyme-linked receptor (including growth factor ) RTK ROR2 ( Robinow syndrome[en.wikipedia.org]

  • Male Pseudohermaphroditism

    Kallmann syndrome: towards molecular pathogenesis. Mol Cell Endocrinol. 2001; 179 75-81 5 de Roux N, Milgrom E. Inherited disorders of GnRH and gonadotropin receptors.[doi.org] Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations.[doi.org]

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