Transient neonatal hypothyroidism probably related to immaturity of thyroidal iodine organification. 1986

O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi

UI MeSH Term Description Entries
D007037 Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. Central Hypothyroidism,Primary Hypothyroidism,Secondary Hypothyroidism,TSH Deficiency,Thyroid-Stimulating Hormone Deficiency,Central Hypothyroidisms,Deficiency, TSH,Deficiency, Thyroid-Stimulating Hormone,Hormone Deficiency, Thyroid-Stimulating,Hypothyroidism, Central,Hypothyroidism, Primary,Hypothyroidism, Secondary,Hypothyroidisms,Primary Hypothyroidisms,Secondary Hypothyroidisms,TSH Deficiencies,Thyroid Stimulating Hormone Deficiency,Thyroid-Stimulating Hormone Deficiencies
D007223 Infant A child between 1 and 23 months of age. Infants
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007455 Iodine A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically. Iodine-127,Iodine 127
D007457 Iodine Radioisotopes Unstable isotopes of iodine that decay or disintegrate emitting radiation. I atoms with atomic weights 117-139, except I 127, are radioactive iodine isotopes. Radioisotopes, Iodine
D003409 Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. Cretinism,Myxedema, Congenital,Endemic Cretinism,Fetal Iodine Deficiency Disorder,Cretinism, Endemic,Hypothyroidism, Congenital
D005260 Female Females
D005500 Follow-Up Studies Studies in which individuals or populations are followed to assess the outcome of exposures, procedures, or effects of a characteristic, e.g., occurrence of disease. Followup Studies,Follow Up Studies,Follow-Up Study,Followup Study,Studies, Follow-Up,Studies, Followup,Study, Follow-Up,Study, Followup
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
January 1994, Annali dell'Istituto superiore di sanita,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
January 1998, Journal of pediatric endocrinology & metabolism : JPEM,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
June 1983, Horumon to rinsho. Clinical endocrinology,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
November 1978, Pediatrics,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
August 1999, Nihon rinsho. Japanese journal of clinical medicine,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
January 1997, Clinical nuclear medicine,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
October 2002, Presse medicale (Paris, France : 1983),
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
January 1958, The Journal of clinical endocrinology and metabolism,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
September 2000, European journal of pediatrics,
O Nose, and T Harada, and K Miyai, and N Hata, and M Ogawa, and I Maki, and S Kanaya, and S Kimura, and K Shimizu, and H Yabuuchi
March 1993, Archives francaises de pediatrie,
Copied contents to your clipboard!