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Klippel–Feil syndrome - Wikipedia, the free encyclopedia
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Klippel–Feil syndrome is a rare disease, ... is that C1-C2 can live a normal life expectancy. Type III — A single open interspace between two fused segments.

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What is Klippel-Feil Syndrome? Klippel-Feil Syndrome is a rare disorder characterized by the congenital fusion of two or more cervical (neck) vertebrae.

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Klippel–Feil syndrome - Wikipedia, the free encyclopedia
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Klippel–Feil syndrome is a rare disease, initially reported in 1884 by Maurice Klippel and André Feil from France, characterized by the congenital fusion of any ...

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Genetics Home Reference Klippel-Feil Syndrome
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Klippel-Trenaunay Syndrome (KTS) Information Page ...
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Klippel-Trenaunay Syndrome (KTS) ... and complications may be life-threatening. However, many individuals can live well while managing their symptoms.

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Klippel-Feil Syndrome : Background, Epidemiology, Etiology
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Klippel-Feil syndrome is detected ... Some patients present early in life with complex cervical and cervicothoracic ... Gjorup L. Klippel-Feil's syndrome.

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Klippel-Trenaunay syndrome - Mayo Clinic
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Klippel Feil syndrome | Disease | Overview | Genetic and ...
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Klippel Feil syndrome (KFS) is a congenital, musculoskeletal condition characterized by the fusion of at least two vertebrae of the neck. Common symptoms ...

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Klippel-Feil syndrome - Pictures, Symptoms, Treatment, Causes
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Klippel-Feil Syndrome | Doctor | Patient
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Klippel–Trénaunay syndrome - Wikipedia, the free encyclopedia
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Klippel–Trénaunay syndrome ... of KTS has limitations and non-surgical approaches need to be developed in order to offer a better quality of life for these patients.

Klippel-Feil Syndrome - WebMD
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Klippel-Trenaunay Syndrome - The Sturge-Weber Foundation
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Klippel-Trenaunay-Weber Syndrome: Facts About Prognosis
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Klippel feil syndrome life expectancy