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19 Possible Causes for Kallmann Syndrome, Parosmia

  • Kallmann Syndrome

    […] version of the IFT88 gene into defective cells in the nose, which restored the cilia and allowed a sense of smell. [35] [36] See also [ edit ] Phantosmia Hyperosmia Hyposmia Parosmia[en.wikipedia.org] 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]

  • Anosmia

    parosmia score measured by QOD correlated with lower TDI values (all P .05).[ncbi.nlm.nih.gov] One of them is Kallmann's syndrome. The condition has been noted to be present in families. It is associated with anosmia and hypogonadism.[ncbi.nlm.nih.gov] OBJECTIVE: To investigate taste, a component of flavor perception, using electrogustometry (EG) in patients with congenital anosmia associated with Kallmann syndrome (KS).[ncbi.nlm.nih.gov]

  • Hyposmia

    parosmia score measured by QOD correlated with lower TDI values (all P .05).[ncbi.nlm.nih.gov] A case of Kallmann syndrome Maria Luisa Cecilia R Arkoncel 1, Francis Raymond P Arkoncel 2, Frances Lina Lantion-Ang 1 1 Section of Endocrinology, Diabetes and Metabolism,[doi.org] See also anosmia, cacosmia, dysosmia, parosmia, specific anosmia. Compare hyperosmia. hyposmic adj.[oxfordreference.com]

  • Uncinate Seizure

    It is used to denote a type of *aura manifesting itself in the form of an * olfactory hallucination or * parosmia (i.e. an olfactory *illusion) … Dictionary of Hallucinations[medicine.academic.ru] Kallmann's Syndrome is the most common cause of congenital olfactory dysfunction, 1/10000-50000), with anosmia (agenesis of the olfactory bulb) and hypogonadotrophic hypogonadism[arquivosdeorl.org.br] In temporal lobe epilepsy, amygdalar and hippocampal lesions cause epigastric discomfort and uncinate fits such as autonomic seizures, psychological seizures, and parosmia[f1000research.com]

  • Olfactory Groove Meningioma

    Anosmia is also a feature of a number of genetic conditions such as Kallmann syndrome (failure to start or finish puberty) and Primary Ciliary Dyskinesia (defect in cilia[teachmeanatomy.info]

  • Parosmia

    In contrast, parosmias always seem to be unpleasant. We report the case of a female with post-infectious hyposmia who reported a pleasant parosmia to selected odorants.[doi.org] Charge syndrome, Kallmann syndrome, Klinefelter's syndrome, Sclerosteosis Hematologic Aneurysm, Aneurysmal subarachnoid hemorrhage, Diabetes mellitus, Pernicious anemia Iatrogenic[wikidoc.org] syndrome, anosmia Psychiatric conditions Anorexia nervosa (not bulimia), major depressive disorder, bipolar disorder, schizophrenia Endocrine conditions Pregnancy, hypothyroidism[aafp.org]

  • Isolated Congenital Anosmia

    Bonfils P, Avan P, Faulcon P, Malinvaud D (2005) Distorted odorant perception: analysis of a series of 56 patients with parosmia.[link.springer.com] Concepts Disease or Syndrome ( T047 ) MSH D017436 ICD10 E23.0 SnomedCT 190559001, 93559003, 33927004 English Syndrome, Kallmann's, Kallmann's Syndrome, Kallmanns Syndrome,[fpnotebook.com] […] cause: loss of smell (anosmia) smelling things that aren't there (phantosmia), like smoke or burnt toast reduced sense of smell (hyposmia) the smell of things to change (parosmia[nhs.uk]

  • Familial Congenital Nasolacrimal Duct Obstruction

    Part of middle1/3 of sternomastoid & tonsil is pused medially " PAROSMIA---PERVERSION OF SMELL," "PHARYNGITIS- MEMBRANOUS---causes--streptococcal, ludwig's angina, diptheria[mypgnotes.com] ) FGFR1 ( Pfeiffer syndrome, KAL2 Kallmann syndrome ) FGFR2 ( Apert syndrome, Antley–Bixler syndrome, Pfeiffer syndrome, Crouzon syndrome, Jackson–Weiss syndrome ) FGFR3[ipfs.io] Jet Lag Syndrome Job's Syndrome Joint Deformities, Acquired Joint Diseases Joint Instability Joint Loose Bodies Kallmann Syndrome Kaposi Varicelliform Eruption Kartagener[medgene.med.harvard.edu]

  • Kallmann Syndrome Type 2

    […] version of the IFT88 gene into defective cells in the nose, which restored the cilia and allowed a sense of smell. [35] [36] See also [ edit ] Phantosmia Hyperosmia Hyposmia Parosmia[en.wikipedia.org] The respective patients are diagnosed with Kallmann syndrome type 2.[symptoma.com] Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency.[ajandrology.com]

  • Juvenile Paralysis Agitans of Hunt

    Ornithinemia (types I, II) Ornithine transcarbamylase deficiency Type 1 Excludes hereditary choroidal dystrophy ( H31.2- ) Hyperosmia R43.1 ICD-10-CM Diagnosis Code R43.1 Parosmia[icd10data.com] Syndrome Kennedy Disease Leber Optic Atrophy And Dystonia Leigh Syndrome Lesch-Nyhan Syndrome Leukodystrophy, Hypomyelinating, 2 Leukodystrophy, Hypomyelinating, 5 Leukodystrophy[familydiagnosis.com] Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of gonadotropin Isolated deficiency of growth hormone Isolated deficiency of pituitary hormone Kallmann's[icd10data.com]

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