Articoli su iris.unipa.it inerenti le malattie rare delle ghiandole endocrine
Ascolta
| Deficienza di ACTH | ACTH deficiency |
| Kallmann sindrome di | Kallmann syndrome |
| Iperaldosteronismi primitivi | Primary aldosteronisms |
| Conn sindrome di | Conn syndrome |
| Iperaldosteronismo primitivo da iperplasia surrenale | Primary aldosteronism due to adrenal hyperplasia |
| Sindromi adrenogenitali congenite | Congenital adrenogenital syndromes |
| 11-beta-idrossilasi deficit di | 11-beta-hydroxylase deficiency |
| 17-alfa-idrossilasi deficit di | 17-alpha-hydroxylase deficiency |
| 18-idrossilasi deficit di | 18-hydroxylase deficiency |
| 20,22-desmolasi deficit di | 20,22-desmolase deficiency |
| 21-idrossilasi deficit di | 21-hydroxylase deficiency |
| 3-beta-idrossi-steroido-deidrogenasi deficit di | 3-beta-hydroxy-steroid dehydrogenase deficiency |
| Citocromo P450 ossidoreduttasi deficit di | Cytochrome P450 oxidoreductase deficiency |
| STAR deficit di | STAR deficiency |
| Deficit congenito isolato di GH | Isolated congenital GH deficiency |
| Ipogonadismo ipogonadotropo congenito | Congenital hypogonadotropic hypogonadism |
| Poliendocrinopatie autoimmuni | Autoimmune polyendocrinopathies |
| Poliendocrinopatia autoimmune tipo I | Autoimmune polyendocrinopathy type I |
| Poliendocrinopatia autoimmune tipo II | Autoimmune polyendocrinopathy type II |
| Poliendocrinopatia autoimmune tipo III | Autoimmune polyendocrinopathy type III |
| Sindromi da resistenza all’ormone della crescita | Growth hormone resistance syndromes |
| Laron sindrome di | Laron syndrome |
| Pubertà precoce idiopatica | Idiopathic precocious puberty |
| Leprecaunismo | Leprechaunism |
| Kenny-Caffey sindrome di | Kenny-Caffey syndrome |
| Refetoff sindrome di | Refetoff syndrome |
| Pendred sindrome di | Pendred syndrome |
| Sindromi da neoplasie endocrine multiple | Multiple endocrine neoplasm syndromes |
| Sindrome MEN tipo 1 | MEN syndrome type 1 |
| Sindrome MEN tipo 2A | MEN syndrome type 2A |
| Sindrome MEN tipo 2B | MEN syndrome type 2B |
| Sindrome MEN tipo 4 | MEN syndrome type 4 |
