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25 Possible Causes for Hypoplastic Testicle, Kallmann Syndrome, Male Hypogonadism

  • Hypogonadotropic Hypogonadism Type 22

    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.[] Kallmann syndrome – absent or impaired puberty.[]

  • Kallmann Syndrome Type 4

    Kallmann syndrome can have a wide variety of additional signs and symptoms.[] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[] […] a b c d e f g h i "Kallmann syndrome".[]

  • Hypogonadotropic Hypogonadism Type 8

    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.[] Male hypogonadism that occur secondary to hypothalamic-pituitary dysfunction is known as hypogonadotropic hypogonadism (HH).[] […] used for the treatment of male hypogonadism.[]

  • Woodhouse Sakati Syndrome

    Hyperpituitarism anterior Acromegaly Hyperprolactinaemia Pituitary ACTH hypersecretion posterior ( SIADH ) general ( Nelson's syndrome ) Hypopituitarism anterior Kallmann[] Our study was performed in a smaller group of male patients with hypogonadism to those that have been reported previously, for two reasons.[] The onset of the disease was in early adolescence, with males showing a more rapid progression. Patients showed alopecia, hypogonadism, and low IGF-1.[]

  • Anorchia

    Conditions associated with hypogonadotropic hypogonadism Kallmann syndrome Anosmia (lack of sense of smell) or hyposmia is a prominent feature of Kallmann syndrome, which[] Figure 1: (a and b) Presence of micropenis and hypoplastic scrotum without testicles Click here to view Case 2 A 15-year-old male was brought by his parents for evaluation[] Gynecomastia How can you classify male hypogonadism into 3 types? memorize this 1.[]

  • Cryptorchidism

    ., hypoplasticity, bifidity, rugae, transposition and pigmentation)? Is the contra-lateral testicle hypertrophic?[] Whereas the duplication mutation has not been reported before, p.Pro26Leu was once observed in a Kallmann syndrome patient.[] Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach. Andrology. 2013; 1:3-16. 18.[]

  • Warburg Micro Syndrome 3

    UPD chr. 14 Kallmann syndrome type 2 FGFR1 Kallmann syndrome type 4 PROK2 Kallmann syndrome type 5 CHD7 KBG syndrome ANKRD11 Keutel syndrome MGP Kleefstra syndrome EHMT1[] Homozygote Humans Hypogonadism Intellectual Disability Male Microcephaly Mutation Optic Atrophy Penis Prognosis RNA Splicing rab3 GTP-Binding Proteins Pub Type(s) Case Reports[] This syndrome was first described by Warburg et al. in a consanguineous Pakistani family with two affected sibs and an affected male cousin (Warburg et al., 1993). 3 Patients[]

  • Prader-Willi Syndrome

    […] or undescended testicles delayed onset of puberty truncal obesity at 1-4 years of age slow motor development may show signs of right-sided heart failure knee and hip instability[] ) FGFR1 (Pfeiffer syndrome, KAL2 Kallmann syndrome) FGFR2 (Apert syndrome, Antley–Bixler syndrome, Pfeiffer syndrome, Crouzon syndrome, Jackson–Weiss syndrome) FGFR3 (Achondroplasia[] Hypogonadism Hypogonadism is a consistent feature of both males and females with PWS.[]

  • Renpenning Syndrome

    (JPS) Juvenile Primary Lateral Sclerosis K Kabuki Syndrome Kallmann Syndrome Kartagener Syndrome Karyotyping: A Special Topic Kawasaki Disease Kearns-Sayre Syndrome (KSS)[] 238320 Leydig cell hypoplasia with pseudohermaphroditism 238320 Luteinizing hormone resistance, female 238320 Precocious puberty, male 176410 LHX3 9q34.3 Pituitary hormone[] TWIST1 and the Saethre-Chotzen Syndrome 64. KAL1, FGFR1, FGF8, PROKR2, PROK2 and Kallmann syndrome 65. TIE2 (TEK) and Venous Malformation 66.[]

  • CHARGE Syndrome

    […] semicircular canals Minor criteria urogenital abnormalities kidney duplex kidney renal hypoplasia / solitary kidney penis hypospadias penile agenesis scrotum/testicles bifid[] 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.[] Julia Rohayem and Eberhard Nieschlag, Central Hypogonadism in the Male: Physiopathology, Diagnosis and Treatment, Hypothalamic-Pituitary Diseases, 10.1007/978-3-319-38681-[]

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