Congenital hypothyroidism: Difference between revisions

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File:CDpic1.png|Congenital hypothyroidism
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File:Cretinnen_aus_Steiermark,_1819_gez._Loder,_gest._Leopold_Müller.jpg|Cretinism in Styria, 1819
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==See Also==
==See Also==
* [[Thyroid]]
* [[Thyroid]]

Latest revision as of 00:29, 27 April 2025

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Congenital hypothyroidism
Jaundice in a newborn, a possible sign of congenital hypothyroidism
Synonyms Cretinism
Pronounce N/A
Specialty N/A
Symptoms Jaundice, poor feeding, constipation, hypotonia, macroglossia, umbilical hernia, prolonged neonatal jaundice
Complications Intellectual disability, growth failure
Onset Neonatal
Duration Lifelong
Types N/A
Causes Thyroid dysgenesis, dyshormonogenesis, iodine deficiency
Risks Family history, maternal iodine deficiency
Diagnosis Newborn screening, thyroid function tests
Differential diagnosis Hypopituitarism, Down syndrome, hypothyroxinemia
Prevention Iodine supplementation during pregnancy
Treatment Levothyroxine
Medication N/A
Prognosis Good with early treatment
Frequency 1 in 2,000 to 4,000 newborns
Deaths N/A


Congenital hypothyroidism is a condition that affects newborns, characterized by an inadequate production of thyroid hormones immediately after birth. This condition can lead to physical and mental growth retardation if not detected and treated promptly.

Etiology[edit]

The most common cause of congenital hypothyroidism is thyroid dysgenesis, where the thyroid gland is either absent, ectopic, or severely underdeveloped. Other causes include dyshormonogenesis, a genetic defect leading to impaired thyroid hormone production, and iodine deficiency.

Clinical Presentation[edit]

Infants with congenital hypothyroidism often appear normal at birth. Symptoms may not be evident until a few weeks after birth and can include jaundice, constipation, poor muscle tone, sluggishness, and a protruding tongue.

Diagnosis[edit]

Diagnosis of congenital hypothyroidism is usually made through newborn screening programs. This involves a heel prick blood test taken within the first few days of life. The test measures the levels of thyroid-stimulating hormone (TSH) and thyroxine (T4) in the infant's blood.

Treatment[edit]

The primary treatment for congenital hypothyroidism is replacement therapy with levothyroxine. This medication is given orally and the dose is adjusted based on regular blood tests to monitor TSH and T4 levels.

Prognosis[edit]

With early diagnosis and appropriate treatment, children with congenital hypothyroidism can lead normal lives. However, if left untreated, the condition can lead to severe intellectual disability and growth failure.

Gallery[edit]

See Also[edit]

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