Primary syringomyelia

Orpha code: 99856OMIM code:

Definition

A rare central nervous system malformation characterized by a fluid-filled longitudinally oriented cavity (syrinx) within the spinal cord, which may or may not communicate with the central canal, does not have an ependymal lining, and is either idiopathic or seen as a familial malformation. Clinical manifestations in symptomatic patients include neuropathic pain, as well as sensory and motor disturbances. Typical presentations may be cape-like loss of pain and temperature sensation along the torso and arms, or disproportionately greater motor impairment in upper compared to lower extremities.

Disease data
Classification

Morphological anomaly

Synonyms
Congenital syringomyelia
Wrodzona jamistość rdzenia
ORPHA code
99856
OMIM code
-
ICD10 code
Q06.4
ICD11 code
8D66.0

No additional description.

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