Zentrale Hypothyreose
Die kongenitale zentrale Hypothyreose ist eine durch Mutationen in verschiedenen Genen ausglöste Hypothyreose ohne kompensatorisch erhöhtem TSH-Spiegel.
Gliederung
Referenzen:
| 1. |
Yamada M et al. (1993) Assignment of human thyrotropin-releasing hormone (TRH) receptor gene to chromosome 8. [^] |
| 2. |
Matre V et al. (1993) Molecular cloning of a functional human thyrotropin-releasing hormone receptor. [^] |
| 3. |
Bonomi M et al. (2009) A family with complete resistance to thyrotropin-releasing hormone. [^] |
| 4. |
Mitnick M et al. (1972) Enzymatic synthesis of thyrotropin releasing hormone (TRH) by hypothalamic "TRH synthetase". [^] |
| 5. |
Foresti V et al. (1985) Central hypothyroidism: isolated thyrotropin-releasing hormone deficiency or resistance of pituitary thyrotropes? [^] |
| 6. |
Katakami H et al. (1984) Hypothalamic hypothyroidism due to isolated thyrotropin-releasing hormone (TRH) deficiency. [^] |
| 7. |
Niimi H et al. (1982) Congenital isolated thyrotrophin releasing hormone deficiency. [^] |
| 8. |
Orphanet article Orphanet ID 99832 [^] |
