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804 Possible Causes for Kallmann Syndrome, Klinefelter Syndrome

  • Endocrine Dysfunction

    Hypogonadism ( Gonadotropin deficiency ) Inherited (genetic and chromosomal) disorders Kallmann syndrome Klinefelter syndrome Turner syndrome Acquired disorders Ovarian failure[en.wikipedia.org] Three of the four PMGCTs patients had the classic form of Klinefelter syndrome.[ncbi.nlm.nih.gov] Men with Klinefelter syndrome often have low testosterone levels. Characteristics of Klinefelter syndrome vary from person to person.[nysopep.org]

  • Puberty Delayed

    I hope to bring together information on Kallmann syndrome (KS) and CHH so it is easily accessible to both patients and clinicians.[delayed-puberty.com] Primary gonadal disorders include absence of the testes, cryptorchidism , Klinefelter syndrome , enzymatic defects in testosterone biosynthesis, and testicular resistance[britannica.com] If Turner syndrome or Klinefelter’s syndrome is suspected then an analysis of the chromosomes will confirm the diagnosis. Imaging can also help with diagnosis.[yourhormones.info]

  • Cryptorchidism

    Whereas the duplication mutation has not been reported before, p.Pro26Leu was once observed in a Kallmann syndrome patient.[ncbi.nlm.nih.gov] We report a case of Klinefelter's syndrome in a 3-year-old boy with unilateral cryptorchidism.[ncbi.nlm.nih.gov] syndrome or mixed gonadal dysgenesis .[en.wikipedia.org]

  • Parosmia

    Charge syndrome , Kallmann syndrome , Klinefelter's syndrome , Sclerosteosis Hematologic Aneurysm , Aneurysmal subarachnoid hemorrhage , Diabetes mellitus , Pernicious anemia[wikidoc.org] syndrome, anosmia Psychiatric conditions Anorexia nervosa (not bulimia), major depressive disorder, bipolar disorder, schizophrenia Endocrine conditions Pregnancy, hypothyroidism[aafp.org] Charge syndrome , Kallmann syndrome , Klinefelter's syndrome , Sclerosteosis Hematologic Aneurysm , Aneurysmal subarachnoid hemorrhage , Diabetes mellitus , Pernicious anemia[wikidoc.org]

  • Male Infertility due to Globozoospermia

    syndrome.[sciencedaily.com] For diseases caused by an abnormal number of chromosomes, such as Klinefelter’s syndrome, it is possible to use PGD to select for normal XX and XY embryos.[thenewatlantis.com] Some of these disorders include Klinefelter’s Syndrome, due to the presence of an extra X chromosome in the male.[ucdenver.edu]

  • Spondyloepimetaphyseal Dysplasia Type Shohat

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] […] punctata Brachytelephalangy-dysmorphism-Kallmann syndrome Brain malformation-congenital heart disease-postaxial polydactyly syndrome Brain-lung-thyroid syndrome Bruck syndrome[se-atlas.de] 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY Syndrome Klinefelter Syndrome 50 Sutton Disease[books.google.com]

  • Syringobulbia

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY Syndrome Klinefelter Syndrome 50 Sutton Disease[books.google.com] 15 Growth Hormone Deficiency 137 Triploidy SyndromePartial Molar Pregnancy 16 HAIRAN Syndrome 138 Turner Syndrome 17 Hermaphroditism True 139 Von HippelLindau Disease 18[books.google.com]

  • X-Linked Hypospadias 1

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] hypogonadism 4 with or without anosmia, 610628 (3)AD75%60PROKR2(O)Hypogonadotropic hypogonadism 3 with or without anosmia, 244200 (3)AD99%61PROP1(O)Pituitary hormone deficiency[nature.com] 47 RothmundThomson Syndrome 37 Trisomy 18 Syndrome 48 Scleromyxedema 38 Syndrome Triple X Syndrome 49 Setleis Syndrome 39 XXY Syndrome Klinefelter Syndrome 50 Sutton Disease[books.google.com]

  • Familial Juvenile Hyperuricemic Nephropathy Type 2

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.de] Kallmann syndrome type 2 FGFR1 Kallmann syndrome type 4 PROK2 Kallmann syndrome, SEMA3A related SEMA3A Laron syndrome GHR Liddle syndrome SCNN1B Liddle syndrome SCNN1G Lipoid[centogene.com] 300804 (JBTS10; OFD1 300170 ) Kallmann-Syndrom 1 308700 (Hypogonadotroper Hypogonadismus mit oder ohne Anosmie 1; ANOS1 ( KAL1 ) 300836 ) Kallmann-Syndrom 2 147950 (Hypogonadotroper[medizinische-genetik-dresden.de]

  • Estradiol

    syndrome.[labcorp.com] Males with sex chromosome genetic conditions such as Klinefelters Syndrome will have a higher level of estradiol.[lowtdoc.com] If the latter occurs in well-nourished children, hypothalamic/pituitary tumors or Kallmann syndrome (or related disorders) should be ruled out.[emedicine.medscape.com]

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