(Q87.1) Congenital malformation syndromes predominantly associated with short stature

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118 733 in individuals diagnosis congenital malformation syndromes predominantly associated with short stature confirmed
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15 317 deaths with diagnosis congenital malformation syndromes predominantly associated with short stature
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13% mortality rate associated with the disease congenital malformation syndromes predominantly associated with short stature

Diagnosis congenital malformation syndromes predominantly associated with short stature is diagnosed Men are 4.38% more likely than Women

61 965

Men receive the diagnosis congenital malformation syndromes predominantly associated with short stature

7 500 (12.1 %)

Died from this diagnosis.

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95
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70
65
60
55
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15
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56 768

Women receive the diagnosis congenital malformation syndromes predominantly associated with short stature

7 817 (13.8 %)

Died from this diagnosis.

Risk Group for the Disease congenital malformation syndromes predominantly associated with short stature - Men and Women aged 0

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In Men diagnosis is most often set at age 0-49, 55-59, 65-69
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Less common in men the disease occurs at Age 50-54, 60-64, 70-95+Less common in women the disease occurs at Age 80-95+
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In Women diagnosis is most often set at age 0-79

Disease Features congenital malformation syndromes predominantly associated with short stature

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Absence or low individual and public risk
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Congenital malformation syndromes predominantly associated with short stature - what does this mean

Congenital malformation syndromes predominantly associated with short stature occur when a person is born with a genetic or chromosomal disorder which causes their body to not grow to the average height of their peers. these syndromes can be caused by a variety of genetic and environmental factors, and can have a range of physical and mental health implications.

What happens during the disease - congenital malformation syndromes predominantly associated with short stature

Congenital malformation syndromes predominantly associated with short stature are caused by genetic mutations that can occur during fetal development. these mutations can affect the growth of bones, organs, and tissues, leading to a range of physical abnormalities and short stature. in some cases, the genetic mutation can be inherited from a parent, while in others it can be a result of a spontaneous mutation. in either case, the mutation can cause a wide range of physical and developmental problems due to the disruption of normal growth and development.

Clinical Pattern

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How does a doctor diagnose

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Treatment and Medical Assistance

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16 Days of Hospitalization Required
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29 Hours Required for Outpatient Treatment

Congenital malformation syndromes predominantly associated with short stature - Prevention

Congenital malformation syndromes predominantly associated with short stature can be prevented by regular prenatal care, including a comprehensive ultrasound to identify any abnormalities, as well as genetic counseling for couples planning to start a family. additionally, avoiding alcohol, drugs, and tobacco use during pregnancy can help reduce the risk of certain types of birth defects.