(E00.2) Congenital iodine-deficiency syndrome, mixed type

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1 891 in individuals diagnosis congenital iodine-deficiency syndrome, mixed type confirmed
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3 599 deaths with diagnosis congenital iodine-deficiency syndrome, mixed type
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190% mortality rate associated with the disease congenital iodine-deficiency syndrome, mixed type

Diagnosis congenital iodine-deficiency syndrome, mixed type is diagnosed Men are 19.51% more likely than Women

1 130

Men receive the diagnosis congenital iodine-deficiency syndrome, mixed type

1 737 (153.7 %)

Died from this diagnosis.

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95
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85
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65
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45
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761

Women receive the diagnosis congenital iodine-deficiency syndrome, mixed type

1 862 (244.7 %)

Died from this diagnosis.

Risk Group for the Disease congenital iodine-deficiency syndrome, mixed type - Men aged 0 and Women aged 30-34

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In Men diagnosis is most often set at age 0-5, 20-24, 60-64
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Less common in men the disease occurs at Age 5-19, 25-59, 65-95+Less common in women the disease occurs at Age 0-29, 35-64, 70-84, 90-95+
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In Women diagnosis is most often set at age 30-34, 65-69, 85-89

Disease Features congenital iodine-deficiency syndrome, mixed type

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Absence or low individual and public risk
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Congenital iodine-deficiency syndrome, mixed type - what does this mean

Congenital iodine-deficiency syndrome, mixed type is a disorder caused by a lack of iodine in the body during fetal development. this deficiency can lead to a range of physical and mental disabilities, including growth delays, hearing problems, and mental retardation. it is most common in areas with limited access to iodine-rich foods and can be prevented with regular iodine supplementation during pregnancy.

What happens during the disease - congenital iodine-deficiency syndrome, mixed type

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Clinical Pattern

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How does a doctor diagnose

  • Physical examination
  • Laboratory tests: Thyroid function tests, Urinalysis, Complete Blood Count (CBC), Stool test for fat absorption, Serum electrolytes, Creatinine, Albumin, and Calcium
  • Imaging tests: Ultrasound of the thyroid, X-ray of the skull and neck
  • Genetic testing
  • Thyroid hormone replacement therapy
  • Iodine supplementation

Treatment and Medical Assistance

Main Goal: Treat the symptoms of Congenital Iodine-Deficiency Syndrome, Mixed Type
  • Prescribe oral iodine supplements.
  • Provide dietary education on iodine-rich foods.
  • Instruct patient to avoid foods high in goitrogens.
  • Monitor thyroid hormone levels.
  • Monitor growth and development.
  • Provide psychosocial support for patient and family.
  • Refer patient to an endocrinologist for further evaluation and treatment.
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22 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Congenital iodine-deficiency syndrome, mixed type - Prevention

The best way to prevent congenital iodine-deficiency syndrome, mixed type is to ensure adequate iodine intake during pregnancy. this can be achieved by ensuring that pregnant women consume a balanced diet that includes foods rich in iodine such as seafood, dairy products, and iodized salt. additionally, pregnant women should take prenatal vitamins that contain iodine.