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19 Possible Causes for Hypoplastic Testicle, Kallmann Syndrome, Osteopenia

  • Hypogonadotropic Hypogonadism Type 8

    Schlüsselwörter Kallmann-Syndrom - hypogonadotroper Hypogonadismus - Anosmie - Genetik Keywords Kallmann’s syndrome - hypogonadotropic hypogonadism - anosmia - genetics[] Decreased testicular size ; Delayed skeletal maturation ; Gonadotropin deficiency ; Gynecomastia ; Hypogonadotrophic hypogonadism ; Hypoplasia of the uterus ; Micropenis ; Osteopenia[] Affiliated tissues include pituitary , olfactory bulb and uterus , and related phenotypes are osteopenia and delayed skeletal maturation Disease Ontology : 12 A hypogonadotropic[]

  • Kallmann Syndrome Type 4

    Kallmann syndrome can have a wide variety of additional signs and symptoms.[] An abdominal CT and DEXA scan revealed undescended testes and osteopenia, respectively. He was diagnosed as IHH.[] […] and psychological disturbances. [5], [6], [7], [8] In addition to being infertile, women with HH suffer from conditions associated with a low estrogenic milieu, including osteopenia[]

  • 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.[] Osteopenia was equally severe in men with immature and mature bone ages, suggesting that abnormal bone development plays an important role in the osteopenia of men with idiopathic[] Women with hypogonadotropic hypogonadism are at a high risk of dislipidemia, urogenital disorders and osteopenia.[]

  • Woodhouse Sakati Syndrome

    Hyperpituitarism anterior Acromegaly Hyperprolactinaemia Pituitary ACTH hypersecretion posterior ( SIADH ) general ( Nelson's syndrome ) Hypopituitarism anterior Kallmann[] […] disease DPM2-CDG Ablepharon macrostomia syndrome Ulna hypoplasia with mental retardation Chromosome 19q13.11 deletion syndrome Spinocerebellar ataxia autosomal recessive 8 Osteopenia[] Hyperpituitarism ( Acromegaly, Hyperprolactinaemia, SIADH ) - Hypopituitarism ( Simmonds' disease / Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes[]

  • 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[] We further highlight osteopenia as a feature of WARBM1.[] SALL4 Jackson-Weiss syndrome FGFR1 Jackson-Weiss syndrome FGFR2 Jawad syndrome RBBP8 Kabuki syndrome type 1 KMT2D Kabuki syndrome type 2 KDM6A Kagami-Ogata syndrome paternal[]

  • Renpenning Syndrome

    (JPS) Juvenile Primary Lateral Sclerosis K Kabuki Syndrome Kallmann Syndrome Kartagener Syndrome Karyotyping: A Special Topic Kawasaki Disease Kearns-Sayre Syndrome (KSS)[] OOA Osteogenesis imperfecta, type I 166200 AD APA Osteopenia and sparse hair 259690 AR(?)[] Prader-willi habitus associated with osteopenia and camptodactyly is known as the urban-rogers-meyer syndrome.[]

  • 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.[] […] stature only, seven with short stature and hypogonadotrophic hypogonadism (HH: delayed puberty, hypoplastic genitalia and/or undescended testis), 12 with HH and one with osteopenia[]

  • Congenital Absence of the Penis

    Testicular fusion: the fusion of the two testicles in the same scrotum [ 2, 5, 20, 21, 22, 23, 24 ] Development abnormalities Microorchidism: small, hypoplastic testicles[] As with a lot (but not all) men with Kallmann syndrome I have underdeveloped genitals.[] […] appetite Panhypopituitarism Microphallus Azoospermia Anterior pituitary hypoplasia Bilateral postaxial polydactyly Ectopic posterior pituitary Depressivity Osteoporosis Osteopenia[]

  • Dubowitz Syndrome

    HYPOPLASTIC LEFT HEART SYNDROME – The right side of the heart pumps blood to the lungs where the blood is oxygenated.[] Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[] Prader-willi habitus associated with osteopenia and camptodactyly is known as the urban-rogers-meyer syndrome.[]

  • Autosomal Dominant Mental Retardation Type 21

    […] left testicle, incoordinated swallowing, rule out genetic syndrome related to hypoplastic facial features, developmental delay, small stature and familial resemblance.[] MLL2 gene P389 Kallmann syndrome, x-linked KAL1 Xp22 P132 Kallmann syndrome FGFR1 8p11.2, GNRHR 8p21, KISSR1 19p13.3, GNRH1, NELF 9q34.3 P133 Laminopathies, Limb-girdle muscular[] Prader-willi habitus associated with osteopenia and camptodactyly is known as the urban-rogers-meyer syndrome.[]

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