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93 Possible Causes for Kallmann Syndrome, Male Hypogonadism, Variable Expressivity within a Family

  • Hypogonadotropic Hypogonadism Type 8

    Schlüsselwörter Kallmann-Syndrom - hypogonadotroper Hypogonadismus - Anosmie - Genetik Keywords Kallmann’s syndrome - hypogonadotropic hypogonadism - anosmia - genetics[thieme-connect.com] First, disease-associated mutations display striking incomplete penetrance and variable expressivity within and across IHH families.[karger.com] Male hypogonadism that occur secondary to hypothalamic-pituitary dysfunction is known as hypogonadotropic hypogonadism (HH).[dnatesting.uchicago.edu]

  • Kallmann Syndrome

    Kallmann syndrome is the result of a genetic defect.[symptoma.com] […] the great variability in clinical expression, even within the same family, as well as the chance, in sporadic cases, of neomutations.[orpha.net] 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]

  • Hypogonadotropic Hypogonadism Type 21

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] […] the great variability in clinical expression, even within the same family, as well as the chance, in sporadic cases, of neomutations.[orpha.net] Fast facts on male hypogonadism Here are some key points about male hypogonadism. More detail is in the main article.[medicalnewstoday.com]

  • Hypogonadotropic Hypogonadism Type 18

    syndrome", abstract "The genetic basis is unknown for 60{\%} of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS).[augusta.pure.elsevier.com] First, disease-associated mutations display striking incomplete penetrance and variable expressivity within and across IHH families.[karger.com] (For presentation in adulthood, see Male Hypogonadism : Symptoms and Signs .)[merckmanuals.com]

  • Anorchia

    Conditions associated with hypogonadotropic hypogonadism Kallmann syndrome Anosmia (lack of sense of smell) or hyposmia is a prominent feature of Kallmann syndrome, which[emedicine.medscape.com] It also demonstrates the variability of the expression of the phenotype within the families.[bmcpediatr.biomedcentral.com] Gynecomastia How can you classify male hypogonadism into 3 types? memorize this 1.[quizlet.com]

  • Laurence Moon Syndrome

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.de] within and between families.[de.slideshare.net] […] in males, renal involvement.[ijmedph.org]

  • 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] Genetic counseling is often delicate for this condition because of the wide variability in clinical expression, both within and between families.[orpha.net] hypogonadism and cardiac conduction defects [ 1 ].[bmcresnotes.biomedcentral.com]

  • Hypogonadotropic Hypogonadism Type 20

    Prognosis - Kallmann syndrome - type 1 Treatment - Kallmann syndrome - type 1 Resources - Kallmann syndrome - type 1[checkorphan.org] […] the great variability in clinical expression, even within the same family, as well as the chance, in sporadic cases, of neomutations.[orpha.net] (For presentation in adulthood, see Male Hypogonadism : Symptoms and Signs .)[merckmanuals.com]

  • Kallmann Syndrome Type 2

    The respective patients are diagnosed with Kallmann syndrome type 2.[symptoma.com] […] the great variability in clinical expression, even within the same family, as well as the chance, in sporadic cases, of neomutations.[orpha.net] Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency.[ajandrology.com]

  • CHARGE Syndrome

    We report on a 14 7/12-year-old Japanese female patient with CHARGE syndrome and CHD7 mutation who also exhibited Kallmann syndrome (KS) phenotype.[ncbi.nlm.nih.gov] CHARGE syndrome shows extremely variable expressivity, even within the same family.[invitae.com] Julia Rohayem and Eberhard Nieschlag, Central Hypogonadism in the Male: Physiopathology, Diagnosis and Treatment, Hypothalamic-Pituitary Diseases, 10.1007/978-3-319-38681-[doi.org]

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