Create issue ticket

458 Possible Causes for Delayed Bone Age, Kallmann Syndrome

  • Kallmann Syndrome

    Kallmann syndrome is the result of a genetic defect.[] A delayed growth or puberty is obvious when the test reveals a bone age lesser than the chronological or actual age of the patients.[] […] a b c d e f g h i "Kallmann syndrome".[]

  • Hypogonadotropic Hypogonadism

    Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[] Furthermore, disturbances of skeletal development may be noted as an overall delayed bone age and a reduced peak bone mass.[] In addition the boy developed delay of puberty, bone age, and closure of the epiphyseal lines of long bones with tall stature.[]

  • Hypogonadotropic Hypogonadism Type 8

    Schlüsselwörter Kallmann-Syndrom - hypogonadotroper Hypogonadismus - Anosmie - Genetik Keywords Kallmann’s syndrome - hypogonadotropic hypogonadism - anosmia - genetics[] 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.[] Anosmia is a distinguishing characteristic of Kallmann syndrome from other subtypes of IHH.[]

  • Primary Male Hypogonadism

    Secondary hypogonadism can be caused by Kallmann syndrome, pituitary or hypothalamic tumors or disorders, obesity, diabetes and Prader-Willi syndrome.[] Delayed bone age (when maturity of the skeleton is behind for your age in years).[] Treatment of Kallmann syndrome with hCG can correct cryptorchidism and establish fertility. Puberty is typically induced using testosterone injectable or gel.[]

  • Delayed Male Puberty

    Gonadotrophin releasing hormone deficiency Kallmann syndrome Hypopituitarism / Hypothyroidism Hypergonadotrophic / Hypogonadism Primary testicular failure.[] […] of exclusion) Consistent findings Delayed Bone Age Family History of Delayed Puberty (75% have parental Pubertal Delay) Consider Jump Start Therapy Indications Girls over[] […] prolactin levels ) Gonadotropin hormone deficiency (Kallmann syndrome) or hormone defect Psychological Stress Anorexia nervosa Physiological Aging Excessive physical exercise[]

  • Male Hypogonadism

    Disorders Causing Pituitary Hypogonadism Brain and pituitary tumors Hemochromatosis Kallmann syndrome Weight loss Obesity Diabetes Testicular Disorders Causing Hypogonadism[] Delayed bone age (when maturity of the skeleton is behind for your age in years).[] Certain conditions such as Kallmann syndrome (abnormal development of the hypothalamus), pituitary disorders, inflammatory diseases, HIV, certain medications, obesity and[]

  • Anterior Pituitary Hypofunction

    syndrome (hypogonadotropic hypogonadism with anosmia) 253.4 Syndrome - see also Disease Kallmann's (hypogonadotropic hypogonadism with anosmia) 253.4 Crosswalk Information[] : delayed fusion of epiphyses; bone growth does not match the age of the child - adults have hypoglycemia: decreased gluconeogenesis; loss of muscle mass; increased adipose[] […] hormone Isolated deficiency of pituitary hormone Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary cachexia[]

  • Hypogonadism

    Polycystic ovary syndrome, and Kallmann syndrome, also called hypogonadotropic hypogonadism. Hemochromatosis and diabetes mellitus can be causes of this as well.[] Delayed bone age (when maturity of the skeleton is behind for your age in years).[] Except the late-onset hypogonadism, classical indications for testosterone supplementation are delayed puberty, Klinefelter syndrome, low bone mass in adult hypogonadism,[]

  • Panhypopituitarism

    Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of gonadotropin Isolated deficiency of growth hormone Isolated deficiency of pituitary hormone Kallmann's[] Furthermore, the hand-wrist X-ray showed delayed bone age [Figure 3], and bone densitometry revealed osteoporosis [total T-score 4.5 (spine) and 3.3 (hip)].[] Also, due to frequent delay in bone age in patients with hypopituitarism, a left hand and wrist radiography are helpful in determining bone age.[]

  • Autosomal-Recessive Robinow Syndrome

    ) FGFR1 ( Pfeiffer syndrome, KAL2 Kallmann syndrome ) FGFR2 ( Apert syndrome, Antley–Bixler syndrome, Pfeiffer syndrome, Crouzon syndrome, Jackson–Weiss syndrome ) FGFR3[] Her bone age was 8 years 5 months at a chronologic age of 10 years.[] Aankyloglossia may contribute to delays in language skill development.[]

Further symptoms

Similar symptoms