KFS, autosomal recessive

Introduction: KFS, autosomal recessive

Description of KFS, autosomal recessive

KFS, autosomal recessive (medical condition): A rare recessively inherited disorder characterized by abnormal fusion of...more »

See also:

Klippel-Feil syndrome recessive type:
  »Introduction: Klippel-Feil syndrome recessive type
  »Symptoms of Klippel-Feil syndrome recessive type

KFS, autosomal recessive: Related Topics

These medical condition or symptom topics may be relevant to medical information for KFS, autosomal recessive:

• Autosomal recessive
• Autosomal recessive disease
• KFS
• Autosomal
• Autosomal diseases
• Recessive
• Recessive diseases

KFS, autosomal recessive as a Disease

KFS, autosomal recessive: Another name for Klippel-Feil syndrome recessive type (or close medical condition association).
  »Introduction: Klippel-Feil syndrome recessive type
  »Symptoms of Klippel-Feil syndrome recessive type

KFS, autosomal recessive: Related Diseases

KFS, autosomal recessive: KFS, autosomal recessive is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Musculoskeletal conditions
• Bone or skeletal conditions
• Congenital conditions
• Congenital conditions - physical defects
• Neck conditions

Symptoms of KFS, autosomal recessive (Klippel-Feil syndrome recessive type)

Some of the symptoms of KFS, autosomal recessive incude:

• Fusion of neck vertebrae
• Short neck
• Low hairline at back of neck
• Restricted neck movement
• Scoliosis

See full list of 29 symptoms of KFS, autosomal recessive (Klippel-Feil syndrome recessive type)

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Bordet-Gengou phenomenon

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