(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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85
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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.

Specified forms of the disease

(M11.0) Hydroxyapatite deposition disease
(M11.1) Familial chondrocalcinosis
(M11.2) Other chondrocalcinosis
(M11.8) Other specified crystal arthropathies
(M11.9) Crystal arthropathy, unspecified