Congenital hypothyroidism risk factors: Difference between revisions

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__NOTOC__
__NOTOC__
{{Congenital hypothyroidism}}
{{Congenital hypothyroidism}}
{{CMG}}
{{CMG}}; {{AE}}
 
==Overview==
==Overview==
==Risk Factors==
==Risk Factors==
[[Mutation]]s in the DUOX2, PAX8, SLC5A5, TG, TPO, TSHB, and TSHR genes result in congenital hypothyroidism.
[[Mutation]]s in the DUOX2, PAX8, SLC5A5, TG, TPO, TSHB, and TSHR genes result in congenital hypothyroidism.
==References==
==References==
{{reflist|2}}
{{reflist|2}}
{{WH}}
 
{{WS}}
[[Category:Congenital disorders]]
[[Category:Endocrinology]]
[[Category:Endocrinology]]
[[Category:Disease]]
[[Category:Disease]]
[[Category:Neonatology]]
 
[[Category:Mature chapter]]
{{WS}}
{{WH}}

Latest revision as of 16:01, 22 July 2016

Congenital hypothyroidism Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Congenital hypothyroidism from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

CT

MRI

Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

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Case #1

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

Risk Factors

Mutations in the DUOX2, PAX8, SLC5A5, TG, TPO, TSHB, and TSHR genes result in congenital hypothyroidism.

References

Template:WS Template:WH