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congenitale hypothyreoïdie door transplacentaire passage van maternaal thyroïdstimulerend hormoonbinding-remmend antilichaam (aandoening)
congenitale hypothyreoïdie door transplacentaire passage van maternaal thyroïdstimulerend hormoonbinding-remmend antilichaam
aangeboren hypothyroïdie door transplacentaire passage van maternaal TSH-binding-inhiberende immunoglobuline
congenitale hypothyreoïdie door transplacentaire passage van thyrotropinebinding-remmend antilichaam van moeder
congenitale hypothyreoïdie door transplacentaire passage van maternaal TSH-binding-remmende antistof
Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibody
A type of transient congenital hypothyroidism a thyroid hormone deficiency that is not permanent. Patients may present with symptoms similar to those of permanent congenital hypothyroidism or they may be asymptomatic. It is caused by the transfer of maternal thyroid stimulating hormone (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. Treatment with l-thyroxine is usually required during this period.
Id717333002
StatusPrimitive
Occurrencecongenitaal
Clinical coursetransitoir
referentieset met complexe 'mapping' naar ICD-10
TargetP72.2
RuleTRUE
AdviceALWAYS P72.2
CorrelationSNOMED CT source code to target map code correlation not specified