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53 Possible Causes for Kallmann Syndrome, Male Hypogonadism, Synkinesia

  • Kallmann Syndrome Type 4

    Synkinesia has been reported in patients with Kallmann syndrome (29,32,33).[78stepshealth.us] Kallmann syndrome can have a wide variety of additional signs and symptoms.[ghr.nlm.nih.gov] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[mayoclinic.org]

  • Kallmann Syndrome

    An X-linked mode of transmission was assumed on the basis of synkinesia and the presence of oligomenorrhoea in the mother.[ncbi.nlm.nih.gov] Kallmann syndrome is the result of a genetic defect.[symptoma.com] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[mayoclinic.org]

  • Hypogonadism

    They often exhibit uncoordinated muscle movements (cerebellar ataxia), or make involuntary movements automatically whenever they make purposeful movements (synkinesia), or[testocreams.com] BACKGROUND: Congenital hypogonadotrophic hypogonadism (CHH) and Kallmann syndrome (KS) are caused by disruption to the hypothalamic-pituitary-gonadal (H-P-G) axis.[ncbi.nlm.nih.gov] MALE HYPOGONADISM 2.[slideshare.net]

  • Hypogonadotropic Hypogonadism Type 8

    Synkinesia (KAL1), dental agenesis (FGF8IFGFR1), digital bony abnormalities (FGF8IFGFR1) and hearing loss (CHD7) can be useful for prioritizing genetic screen [ 6 ].[omicsonline.org] Kallmann syndrome - absent puberty with no sense of smell. Me at 18 years old in my final year at school. I had not started puberty yet.[imgur.com] Male hypogonadism that occur secondary to hypothalamic-pituitary dysfunction is known as hypogonadotropic hypogonadism (HH).[dnatesting.uchicago.edu]

  • Kallmann Syndrome Type 3

    Synkinesia (KAL1), dental agenesis (FGF8IFGFR1), digital bony abnormalities (FGF8IFGFR1) and hearing loss (CHD7) can be useful for prioritizing genetic screen [ 6 ].[omicsonline.org] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Gynecomastia How can you classify male hypogonadism into 3 types? memorize this 1.[quizlet.com]

  • Ichthyosis and Male Hypogonadism

    His family medical records showed no history of delayed development, synkinesia or renal, dental, mental or neurologic abnormalities.[edmcasereports.com] Kallmann syndrome.[emedicine.medscape.com] Homepage Rare diseases Search Search for a rare disease Ichthyosis-male hypogonadism syndrome ORPHA:431 Synonym(s): - Prevalence: - Inheritance: - Age of onset: - ICD-10:[orpha.net]

  • Hypogonadotropic Hypogonadism

    In Kallmann syndrome (KS), according to the presence of certain accompanying clinical features, genetic screening for particular gene(s) may be prioritized: synkinesia (KAL1[ncbi.nlm.nih.gov] Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] Abstract Male hypogonadism is defined as the deficiency of testosterone or sperm production synthesized by testicles or the deficiency of both.[ncbi.nlm.nih.gov]

  • Hypogonadotropic Hypogonadism Type 18

    Synkinesia (KAL1), dental agenesis (FGF8IFGFR1), digital bony abnormalities (FGF8IFGFR1) and hearing loss (CHD7) can be useful for prioritizing genetic screen [ 6 ].[omicsonline.org] syndrome", abstract "The genetic basis is unknown for 60{\%} of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS).[augusta.pure.elsevier.com] (For presentation in adulthood, see Male Hypogonadism : Symptoms and Signs .)[merckmanuals.com]

  • Hypogonadotropic Hypogonadism Type 22

    […] include a small penis or undescended testicles in males, kidney abnormalities, cleft lip and/or palate, clubfoot, hearing problems, and central nervous system problems such as synkinesia[healthofchildren.com] Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2). Hum Mutat 2005;25:98–9. PubMed Crossref Google Scholar 3.[degruyter.com] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[mayoclinic.org]

  • Delayed Male Puberty

    As well as cryptorchidism, associated features include micropenis, synkinesia (mirror movements), cleft lip and palate, dental agenesis, skeletal anomalies and hearing loss[patient.info] Gonadotrophin releasing hormone deficiency Kallmann syndrome Hypopituitarism / Hypothyroidism Hypergonadotrophic / Hypogonadism Primary testicular failure.[rcpa.edu.au] Now in a revised second edition, this comprehensive text covers all aspects of male hypogonadism from the basic science to clinical management, comprehensively explaining[books.google.com]

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