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(Z83.4) Family history of other endocrine, nutritional and metabolic diseases
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35 669 in individuals diagnosis family history of other endocrine, nutritional and metabolic diseases confirmed
Diagnosis family history of other endocrine, nutritional and metabolic diseases is diagnosed Men are 6.77% more likely than Women
19 042
Men receive the diagnosis family history of other endocrine, nutritional and metabolic diseases
0 (less than 0.1%)Died from this diagnosis.
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16 627
Women receive the diagnosis family history of other endocrine, nutritional and metabolic diseases
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease family history of other endocrine, nutritional and metabolic diseases - Men and Women aged 0
In Men diagnosis is most often set at age 0-19, 60-74
Less common in men the disease occurs at Age 20-59, 75-95+Less common in women the disease occurs at Age 20-24, 30-34, 45-95+
In Women diagnosis is most often set at age 0-19, 25-29, 35-44
Disease Features family history of other endocrine, nutritional and metabolic diseases
Absence or low individual and public risk
Family history of other endocrine, nutritional and metabolic diseases - what does this mean
Family history of other endocrine, nutritional and metabolic diseases is a risk factor for a variety of diseases. these diseases are caused by a combination of genetic and environmental factors, and can include diabetes, obesity, thyroid disorders, and other metabolic disorders. the risk of developing these conditions increases if there is a family history of these diseases. therefore, it is important to be aware of your family history and to take steps to reduce your risk of developing such diseases.
What happens during the disease - family history of other endocrine, nutritional and metabolic diseases
The pathogenesis of this disease is likely to be multifactorial, involving genetic, environmental, and lifestyle factors. it is likely that individuals with a family history of other endocrine, nutritional, and metabolic diseases are more likely to be predisposed to this condition due to a combination of inherited genetic mutations, epigenetic changes, and environmental exposures. these factors can lead to dysregulation of hormones, metabolic pathways, and other physiological processes, resulting in the development of this disease.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Blood tests
- Urine tests
- Imaging studies
- Genetic testing
- Thyroid function tests
- Adrenal function tests
- Pituitary function tests
- Ovarian function tests
- Growth hormone tests
- Glucose tolerance tests
- Lipid profile tests
- Bone density tests
Treatment and Medical Assistance
Main Goal of the Treatment: To treat the family history of other endocrine, nutritional and metabolic diseases.
- Educating family members and caregivers about endocrine, nutritional and metabolic diseases.
- Regular monitoring of family members for signs and symptoms of endocrine, nutritional and metabolic diseases.
- Developing a plan of action for family members who are diagnosed with endocrine, nutritional and metabolic diseases.
- Encouraging family members to adopt healthy lifestyle habits, such as eating a balanced diet and exercising regularly.
- Encouraging family members to seek medical advice when necessary.
- Seeking out support from other families with similar endocrine, nutritional and metabolic diseases.
- Utilizing medical treatments and therapies as recommended by a doctor.
8 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Family history of other endocrine, nutritional and metabolic diseases - Prevention
In order to prevent a family history of other endocrine, nutritional and metabolic diseases, it is important to maintain a healthy lifestyle, including regular exercise, a balanced diet, and regular check-ups with a doctor. it is also important to be aware of any family history of endocrine, nutritional and metabolic diseases, and to take steps to reduce the risk of developing these conditions.