(Q76.1) Klippel-feil syndrome

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83 440 in individuals diagnosis klippel-feil syndrome confirmed
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2 268 deaths with diagnosis klippel-feil syndrome
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3% mortality rate associated with the disease klippel-feil syndrome

Diagnosis klippel-feil syndrome is diagnosed Women are 1.48% more likely than Men

41 103

Men receive the diagnosis klippel-feil syndrome

1 496 (3.6 %)

Died from this diagnosis.

100
95
90
85
80
75
70
65
60
55
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45
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15
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5
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42 337

Women receive the diagnosis klippel-feil syndrome

772 (1.8 %)

Died from this diagnosis.

Risk Group for the Disease klippel-feil syndrome - Men aged 15-19 and Women aged 10-14

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In Men diagnosis is most often set at age 0-74, 85-89
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Less common in men the disease occurs at Age 75-84, 90-95+Less common in women the disease occurs at Age 70-74, 80-84, 90-95+
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In Women diagnosis is most often set at age 0-69, 75-79, 85-89

Disease Features klippel-feil syndrome

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Absence or low individual and public risk
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Klippel-feil syndrome - what does this mean

Klippel-feil syndrome is a congenital condition caused by the fusion of two or more vertebrae in the cervical spine. this fusion can cause a short neck, a low hairline at the back of the head, and restricted movement of the neck. other common symptoms include scoliosis, hearing loss, and heart and kidney defects.

What happens during the disease - klippel-feil syndrome

Klippel-feil syndrome is a rare congenital disorder that is caused by the abnormal development and fusion of the cervical vertebrae in the neck. this fusion can lead to decreased range of motion in the neck and head, as well as a short neck and low hairline. it can also be associated with other skeletal abnormalities, such as scoliosis and abnormalities in the ribs and shoulder blades. in some cases, there may be neurological problems due to pressure on the spinal cord and nerve roots.

Clinical Pattern

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How does a doctor diagnose

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Treatment and Medical Assistance

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14 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Klippel-feil syndrome - Prevention

Klippel-feil syndrome is a congenital disorder and, as such, there is no known way to prevent it. however, early diagnosis and treatment can help reduce the severity of the symptoms and can improve the quality of life for those affected. regular check-ups with a healthcare provider can help to identify any potential issues and allow for early intervention.