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Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies
Disease definition
Congenital hypothyroidism due to transplacental passage of maternal thyroid-stimulating hormone (TSH)-binding inhibitory antibodies is a type of transient congenital hypothyroidism (see this term), a thyroid hormone deficiency that is not permanent.
ORPHA:95715
Classification level: Disorder- Synonym(s): -
- Prevalence: 1-9 / 100 000
- Inheritance: Not applicable
- Age of onset: Neonatal
- ICD-10: P72.2
- OMIM: -
- UMLS: C4273914
- MeSH: -
- GARD: -
- MedDRA: -
Summary
Epidemiology
Prevalence is estimated to be 1/100,000.
Clinical description
Patients may present with symptoms similar to those of permanent CH (see this term) or they may be asymptomatic.
Etiology
It is caused by the transfer of maternal TSH blocking antibodies, which can block the TSH receptor in the neonatal thyroid resulting in hypothyroidism in the infant. The effect can last up to 3-6 months after birth as maternal antibody levels fall.
Management and treatment
Treatment with l-thyroxine is usually required during this period.
A summary on this disease is available in Deutsch (2010) Español (2010) Français (2010) Italiano (2010) Nederlands (2010) Português (2010)
Detailed information
Guidelines
- Anesthesia guidelines
- Czech (2017) - Orphananesthesia
- English (2017) - Orphananesthesia
- Español (2017) - Orphananesthesia
Disease review articles
- Review article
- English (2010) - Orphanet J Rare Dis


Additional information