Congenital Hypothyroidism [kongenitální hypotyreóza]
- Terms
-
endemický kretenismus
hypotyreóza kongenitální
kongenitální hypotyreoidismus
kretenismus
myxedém kongenitální
vrozená hypotyreóza
-
Cretinism
Endemic Cretinism
Fetal Iodine Deficiency Disorder
Myxedema, Congenital
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.
- DUI
- D003409 MeSH Browser
- CUI
- M0005308
- History note
- 2006 (1966)
- Public note
- 2006; see CRETINISM 1966-2005
Allowable subheadings
- BL
- blood 9
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 1
- CO
- complications 4
- DI
- diagnosis 38
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 16
- EC
- economics
- EM
- embryology 1
- EN
- enzymology
- EP
- epidemiology 13
- EH
- ethnology
- ET
- etiology 16
- GE
- genetics 9
- HI
- history 3
- IM
- immunology
- ME
- metabolism 6
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 4
- PP
- physiopathology 4
- PC
- prevention & control 13
- PX
- psychology 2
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 9
- UR
- urine
- VE
- veterinary
- VI
- virology
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Hypothyroidism, Congenital, Nongoitrous, 3 Disease MeSH Browser
Hypothyroidism, Congenital, Nongoitrous, 5 Disease MeSH Browser
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Thyroid Dyshormonogenesis 1 Disease MeSH Browser
Thyroid Dyshormonogenesis 2A Disease MeSH Browser
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