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congenital hypothyroidism

   Also found in: Dictionary/thesaurus, Encyclopedia, Wikipedia, Hutchinson 0.03 sec.
hypothyroidism
deficiency of thyroid gland activity, with underproduction of thyroxine, or the condition resulting from it. Common in adult dogs, particularly certain breeds, as a result of an idiopathic atrophy of the thyroid or a lymphocytic thyroiditis. Alopecia, weight gain, mental dullness, fatigue, cold intolerance, infertility and neurological deficits are seen. In food animals the syndrome is classical neonatal colloid goiter. See also goiter.

autoimmune hypothyroidism
see lymphocytic thyroiditis.
congenital hypothyroidism
results from congenital thyroid dysgenesis, defective hormone synthesis or severe iodine deficiency. There is dwarfism, macroglossia and mental dullness.
iatrogenic hypothyroidism
may follow treatment for hyperparathyroidism in cats.
juvenile hypothyroidism
congenital hypothyroidism (above).
primary hypothyroidism
that resulting from disease of the thyroid glands.
secondary hypothyroidism
caused by a deficiency of thyroid-stimulating hormone, usually as a result of a lesion in the pituitary gland.
tertiary hypothyroidism
caused by a lack of synthesis or release of thyrotropin releasing hormone.

congenital hypothyroidism
Congenital myxedema, cretinism Hypothyroidism of neonatal onset, which occurs in 1/±7000 births, more commonly in ♀, characterized by mental and physical retardation due to inappropriate thyroid development or inadequate maternal intake of iodine during gestation. See Myxedema.


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] was tested in 1997 and 1998, we evaluated the prevalence of primary congenital hypothyroidism (PCH) and high thyroid-stimulating hormone (TSH) levels among the 342,257 California newborns screened in 1998.
The prevalence of this disease is 1 in 30,000 to 50,000 live births, and it is the second most common cause (10 to 15%) of permanent congenital hypothyroidism.
In Brazil (170 million persons and approximately 2,400,000 newborns/year), the prevalence of infectious diseases is higher than phenylketonuria (1 in 13,000) and congenital hypothyroidism (1 in 3,500).
 
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congenital hypoplastic anemia
congenital hypoplastic anemia
congenital hypoplastic anemia
congenital hypoplastic anemia
congenital hypothyroid dysmaturity syndrome
congenital hypothyroidism
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congenital hypotrichosis
congenital hypotrichosis
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congenital hypotrichosis universalis
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congenital ichthyosiform erythroderma
congenital ichthyosiform erythroderma
congenital ichthyosiform erythroderma
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congenital immunity
congenital immunodeficiency
congenital immunodeficiency
congenital immunodeficiency
congenital immunodeficiency
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Congenital insensitivity to pain with anhidrosis
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