OMIA:000536-9925 : Hypothyroidism, congenital in Capra hircus (goat)
Links to MONDO diseases:
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Deficiency of thyroid gland activity. Also known as Goiterous congenital hypothyroidism; Congenital hypothyroidism; Thyroid dyshormonogenesis. This disorder can be caused by mutations in different genes, and forms of the disease exist that are not inherited.
Cite this entry
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
|1997||Piosik, P.A., Vangroenigen, M., Vandoorn, J., Baas, F., Devijlder, J.J.M. :|
|Effects of maternal thyroid status on thyroid hormones and growth in congenitally hypothyroid goat fetuses during the second half of gestation Endocrinology 138:5-11, 1997. Pubmed reference: 8977378 .|
|1996||Piosik, P.A., Vangroenigen, M., Baas, F. :|
|Effect of thyroid hormone deficiency on RC3/Neurogranin mRNA expression in the prenatal and adult caprine brain Molecular Brain Research 42:227-235, 1996. Pubmed reference: 9013778 .|
|1995||Piosik, P.A., Vangroenigen, M., Ponne, N.J., Bolhuis, P.A., Baas, F. :|
|RC3 neurogranin structure and expression in the caprine brain in relation to congenital hypothyroidism Molecular Brain Research 29:119-130, 1995. Pubmed reference: 7539519 .|
- Created by Frank Nicholas on 06 Sep 2005