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1,538 Possible Causes for Anosmia, Luteinizing Hormone Low, SMMCI

  • Hypogonadotropic Hypogonadism Type 22

    BACKGROUND: Congenital hypogonadotropic hypogonadism (CHH) is classified as Kallmann syndrome (KS) with anosmia/hyposmia or normosmic (n)CHH.[] PubMed Single central maxillary incisor and holoprosencephaly. Single central maxillary incisor and holoprosencephaly. Am J Med Genet. 1987 Oct;28(2):483-7.[] His laboratory investigations showed low luteinizing hormone (LH), follicle stimulating hormone (FSH), and testosterone levels.[]

  • Nasal Obstruction

    In this paper we report a 27-year-old Caucasian woman with a calcified mass in the right nasal cavity causing nasal obstruction, anosmia and facial pain.[] But in many cases the diagnosis is late, when the patient seeks medical service for long time ago unilateral nasal obstruction, anosmia and rhinorrhea.[] The importance of olfaction is perhaps best appreciated by realizing the unpleasant effects of anosmia, like the inability to enjoy the smell of food and secondary decrease[]

    Missing: Luteinizing Hormone Low
  • Kallmann Syndrome

    OBJECTIVE: Kallmann syndrome (KS) is a genetic disorder with the distinctive features of hyposmia or anosmia and hypogonadotropic hypogonadism.[] Serum luteinizing hormone levels were low or normal.[] As an adult, while untreated, he had subnormal levels of serum testosterone, low gonadotropins, and normal response to luteinizing hormone- releasing hormone.[]

    Missing: SMMCI
  • Hypogonadotropic Hypogonadism

    Neuroendocrinology: PDF Only Abstract Kallmann's syndrome is a form of idiopathic hypogonadotropic hypogonadism (IHH) associated with hyposmia or anosmia.[] Hormonal evaluation showed very low levels of gonadotropins, luteinizing hormone-releasing hormone test (LHRH test) and sexual steroids in both patients, suggesting a possible[] The association of anosmia and congenital hypogonadotropic hypogonadism (CHH) is well described; however, congenital arhinia is a malformation associated with CHH that occurs[]

    Missing: SMMCI
  • Hypogonadotropic Hypogonadism Type 18

    Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts.[] Isolated gonadotropin-releasing hormone (GnRH) deficiency (IGD) is characterized by inappropriately low serum concentrations of the gonadotropins LH (luteinizing hormone)[] Investigations: Serum levels of testosterone and luteinizing hormone were low.[]

    Missing: SMMCI
  • Upper Respiratory Infection

    Only one of the included papers examined the effect of saline irrigation on other symptoms, such as anosmia (loss of the sense of smell) and cough associated with acute URTIs[]

    Missing: Luteinizing Hormone Low SMMCI
  • Hypogonadotropic Hypogonadism Type 8

    Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts.[] Further diagnostic tests revealed low testosterone concentrations (0.958 ng/ml; reference range 1.8 – 7.58 ng/ml) and low luteinizing hormone (LH) concentrations ( Treatment[] Online Letters: Observations Subnormal testosterone concentrations have been found in 25% of men with type 2 diabetes in association with inappropriately low luteinizing hormone[]

    Missing: SMMCI
  • Luteinizing Hormone Deficiency

    This disorder featuring lack of sense of smell is called anosmia or Kallmann syndrome.[] Other disorders of hypothalamus which affect secretion of gonadotropin releasing hormone can cause low level of luteinizing hormone.[] Two thirds of the time, this is associated with anosmia (ie, Kallmann syndrome).[]

    Missing: SMMCI
  • Kallmann Syndrome Type 4

    Kallmann syndrome (KS) is a rare genetic disorder characterized by hypogonadotropic hypogonadism associated with anosmia or hyposmia.[] […] and luteinizing hormone production.[] […] hypogonadotropic hypogonadism and anosmia hypogonadotropic hypogonadism-anosmia syndrome Kallman's syndrome Balasubramanian R, Crowley WF Jr.[]

    Missing: SMMCI
  • Hypogonadism

    […] eunuchoidism, male hypogonadism the state of being a eunuch (either because of lacking testicles or because they failed to develop) Kallman's syndrome hypogonadism with anosmia[] hormone ( 9.4 mU/mL)], secondary (low total testosterone, low/normal luteinizing hormone), primary (low total testosterone, elevated luteinizing hormone) and compensated[] Two subtypes of IHH have been defined: Kallmann syndrome (CHH with anosmia; see this term) mainly associated with abnormal embryonic migration of the Gn-releasing hormone[]

    Missing: SMMCI

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