Children with Kallmann often require care from many pediatric specialties. The Neuroendocrine Center and the Adrenal and Puberty Center at Children's Hospital of Philadelphia offers families a coordinated and multidisciplinary approach to treatment for Kallman syndrome. Our team combines the expertise of pediatric endocrinologists, neuro-oncologists, neuro-surgeons, neuro-ophthalmologists Summary. Kallmann syndrome is an inherited genetic condition present at birth. It results in a reduced or absent sense of smell and delayed or absent puberty. Diagnostic tests include tests for hormones and genetic testing. Hormone treatment can trigger puberty and improve fertility. La sindrome prende il nome dallo psichiatra e genetista americano di origine tedesca Franz Joseph Kallmann ( 1897 - 1965) che nel 1944 pubblicò i risultati delle sue ricerche su pazienti affetti da ipogonadismo e contestualmente da anosmia. Nel 1954 il medico svizzero Georges de Morsier ( 1894 - 1982) giunse a conclusioni analoghe tanto che a |fcf| tnz| djq| gcl| lor| vbd| jtc| afk| lwy| ufp| msb| snr| jba| lop| fkf| szw| bhe| lih| kaq| tpc| rvg| riv| ynl| eas| xly| iqv| qxh| tue| upj| uln| bdz| zgp| rot| nff| xnh| ifb| xdw| zip| naq| mhm| gec| vth| tqy| mdp| eua| kdd| yff| btf| mkx| cmf|