Possible Causes For Paraplegia, spastic hereditary - Causes

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Hereditary, Familial, Genetic Disorders

Paraplegia, spastic hereditary

Laurence-Moon-Biedel syndrome

Synonyms

CHARCOT-MARIE-TOOTH DISEASE WITH PYRAMIDAL FEATURES AUTOSOMAL DOMINANT, CHARCOT-MARIE-TOOTH NEUROPATHY WITH PYRAMIDAL FEATURES AUTOSOMAL DOMINANT, CMT WITH PYRAMIDAL FEATURES, congenital paraplegia spastic, familial paralysis spastic, FAMILIAL SPASTIC PARAPLEGIA AUTOSOMAL DOMINANT 1, Familial spastic paraplegia syndrome, FSP1, Hered mtr/sen neurop pyr sgn, Heredit motr/sens neuropathy V, Hereditary motor and sensory neuropathy type V, HEREDITARY MOTOR AND SENSORY NEUROPATHY V, Hereditary Motor Sensory Neuropathy with Pyramidal Signs, Hereditary motor-sensory neuropathy with pyramidal signs, Hereditary sensory-motor neuropathy type 5, Hereditary sensory-motor neuropathy type V, Hereditary sensory-motor neuropathy type V (disorder), Hereditary spastic paraplegia, Hereditary spastic paraplegia (disorder), Hereditary Spastic Paraplegias, HMSN Type V, HMSN V, HMSN V (Hereditary Motor and Sensory Neuropathy Type V), HMSN5, HSMN V, HSP Heredit spast paraplegia, HSP Hereditary spastic paraplegia, Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia, Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia, paralysis familial spastic, paralysis spastic familial, paralysis spastic hereditary, PARALYSIS SPASTIC SPINAL FAMILIAL, Paraplegia Hereditary Spastic, PARAPLEGIA SPASMODIC INFANTILE, PARAPLEGIA SPASTIC CONGENITAL, Paraplegias Hereditary Spastic, PERONEAL MUSCULAR ATROPHY WITH PYRAMIDAL FEATURES AUTOSOMAL DOMINANT, Spastic congenital paraplegia, spastic paralysis familial, spastic paralysis hereditary, SPASTIC PARAPLEGIA 3 AUTOSOMAL DOMINANT, Spastic Paraplegia Hereditary, Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy, Spastic paraplegia with hypertrophic motor-sensory neuropathy type 5, Spastic paraplegia with hypertrophic sensory-motor neuropathy type V, Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy, Spastic Paraplegias Hereditary, SPG3, SPG3A, STRUMPELL DISEASE, Strumpell-Lorrain disease, Strumpell's disease, Type V Hereditary Motor and Sensory Neuropathy, Type V HMSN

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