Klippel Feil syndrome dominant type

Overview

Klippel-Feil syndrome, dominant type: A rare dominantly inherited disorder characterized by abnormal fusion of two or more vertebrae in the neck. The disorder is often associated with other abnormalities but their incidence is highly variable.

Symptoms

The list of signs and symptoms mentioned in various sources for Klippel-Feil syndrome, dominant type includes the 29 symptoms listed below: * Fusion of neck vertebrae * Short neck * Low hairline at back of neck * Restricted neck movement * Scoliosis * Spina bifida * Kidney anomalies * Rib anomalies * Cleft palate * Respiratory problems * Heart malformations * Head abnormalities * Face abnormalities * Skeleton abnormalities * Sex organ abnormalities * Muscle abnormalities * Brain abnormalities * Spinal cord abnormalities * Arm abnormalities * Leg abnormalities * Finger abnormalities * Cranial nerve palsy * Cervical nerve palsy * Synkinesia * Deafness * Ventricular septal defect * Mental deficiency * Sprengel anomaly * Posterior fossa dermoid cysts Note that Klippel-Feil syndrome, dominant type symptoms usually refers to various symptoms known to a patient, but the phrase Klippel-Feil syndrome, dominant type signs may refer to those signs only noticable by a doctor.

Causes

* Brain abnormalities * Cleft palate * Cranial nerve palsy * Deafness * Fusion of neck vertebrae * Kidney anomalies * Low hairline at back of neck * Mental deficiency * Respiratory problems * Scoliosis * Short neck * Spina bifida

Diagnosis

The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Klippel-Feil syndrome, dominant type. This medical information about signs and symptoms for Klippel-Feil syndrome, dominant type has been gathered from various sources, may not be fully accurate, and may not be the full list of Klippel-Feil syndrome, dominant type signs or Klippel-Feil syndrome, dominant type symptoms. Furthermore, signs and symptoms of Klippel-Feil syndrome, dominant type may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Klippel-Feil syndrome, dominant type symptoms.