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45 Possible Causes for Frontal Headache, Kallmann Syndrome, Male Hypogonadism

  • Hypogonadism

    BACKGROUND: Congenital hypogonadotrophic hypogonadism (CHH) and Kallmann syndrome (KS) are caused by disruption to the hypothalamic-pituitary-gonadal (H-P-G) axis.[] MALE HYPOGONADISM 2.[] Kallmann syndrome) as well as normal puberty that is accompanied by an altered reproductive system later in life (i.e. ...[]

  • Hypogonadotropic Hypogonadism Type 22

    headaches with vomiting 2.[] Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2). Hum Mutat 2005;25:98–9. PubMed Crossref Google Scholar 3.[] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[]

  • Empty Sella Syndrome

    ) FGFR1 ( Pfeiffer syndrome, KAL2 Kallmann syndrome ) FGFR2 ( Apert syndrome, Antley–Bixler syndrome, Pfeiffer syndrome, Crouzon syndrome, Jackson–Weiss syndrome ) FGFR3[] Headache Happiness Headache Happiness! Stop Your Headache BEFORE IT STARTS. How To Get Rid Of Your Headache BEFORE It Starts![] CASR ( Familial hypocalciuric hypercalcemia ) Class F FZD4 ( Familial exudative vitreoretinopathy 1 ) Enzyme-linked receptor (including growth factor ) RTK ROR2 ( Robinow syndrome[]

  • Pituitary Disorder

    Headache Patients with macroadenomas often have frontal, forehead and temporal area headaches. Pituitary adenoma removal often results in headache resolution.[] Hyperpituitarism anterior Acromegaly Hyperprolactinaemia Pituitary ACTH hypersecretion posterior ( SIADH ) general ( Nelson's syndrome ) Hypopituitarism anterior Kallmann[] hypogonadism.[]

  • Boucher-Neuhäuser Syndrome

    Patients may also present with dysmetria, frontal headaches, and pes cavus.[] Kallmann Syndrome : Inherited syndrome characterized by hypogonadotropic hypogonadism and anosmia caused by agenesis of the olfactory bulbs, often combined with other birth[] Now in a revised second edition, this comprehensive text covers all aspects of male hypogonadism from the basic science to clinical management, comprehensively explaining[]

  • Hyposmia

    Patient 2 A 49-year-old African-American female patient presented with altered flavor perception and frontal headaches. She did not have specific olfactory complaints.[] 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,[] Two males, 9-11 and 29-31 years of age, with severe hypoplasia of the nose, hypoplasia of the eyes, sensory abnormalities of taste and smell, and hypogonadism were studied[]

  • Autoimmune Hypophysitis

    A 46-year-old man presented with frontal headache, a visual field defect and general fatigue.[] KAL-1 gene encodes a protein named ANOSMINE -1 a nerve-adhesion protein that is not present in nasal epithelium and hypothalamus in Kallmann’s syndrome DIAGNOSTIC: T, LH,[] Case 2, male 54 years. MRI volume: AP 13.5 mm, CC 7.7 mm. Hormonal assessment: central hypothyroidism, hypoadrenalism, hypogonadism, GH deficiency, hyperprolactinemia.[]

  • Anterior Pituitary Hypofunction

    Headache localized in the frontal region, the orbital and temporal regions. It is of a throbbing character. Pain often monotonous.[] syndrome (hypogonadotropic hypogonadism with anosmia) 253.4 Syndrome - see also Disease Kallmann's (hypogonadotropic hypogonadism with anosmia) 253.4 Crosswalk Information[] hypogonadism, and estradiol for female hypogonadism (usually with a progestogen to inhibit unwanted effects on the uterus ).[]

  • Hypohidrotic Ectodermal Dysplasia

    Other symptoms: Headache, cognitive impairment with frontal syndrome, memory loss or dementia, paresis and motor symptoms, sensory symptoms such as dysesthesia, paresthesia[] syndrome Kaler Garrity Stern Syndrome Kallmann syndrome Kantaputra Gorlin Syndrome Kaplan Plauchu Fitch Syndrome Kaplowitz Bodurtha syndrome Kapur Toriello Syndrome Karak[] (LADD) p. 57 Kallmann Syndrome (KS; KAL2) p. 59 Other Pathways p. 62 Bloom Syndrome (BS, BLS) p. 63 p. 65 Diastrophic Dysplasia Syndrome p. 67 Johanson-Blizzard Syndrome[]

  • Delayed Menarche

    […] compression of the optic nerve and/or chiasma - bitemporal inferior quadrantinopia progressing to bitemporal hemianopia; optic atrophy -mild to severe dementia - due to frontal[] Other causes for delayed puberty may be due to Kallmann Syndrome.[] "Treatment of hypogonadism in males". Pediatric Endocrinology Reviews . 11 Suppl 2: 230–9. PMID 24683947 . Legato MJ , ed. (2004).[]

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