to cause the disorder. Other Names for This Condition Autosomal dominant spastic paraplegia 31 Spastic paraplegia 31

Spastic paraparesis type 2 Spastic paraplegia 2 SPG2 X-linked spastic paraplegia 2 X-linked spastic paraplegia type 2 Additional Information

of all spastic paraplegia cases. Causes Mutations in the SPG7 gene cause spastic paraplegia type 7. The

Resources Genetic Testing Information Genetic Testing Registry: Hereditary spastic paraplegia 4 Genetic Testing Registry: Hereditary spastic paraplegia Genetic and Rare

to cause the disorder. Other Names for This Condition Autosomal dominant spastic paraplegia 31 Spastic paraplegia 31

symptoms of the condition. Other Names for This Condition Autosomal recessive spastic paraplegia 5A Spastic paraplegia 5A

of all spastic paraplegia cases. Causes Mutations in the SPG7 gene cause spastic paraplegia type 7. The

Resources Genetic Testing Information Genetic Testing Registry: Hereditary spastic paraplegia 4 Genetic Testing Registry: Hereditary spastic paraplegia Genetic and Rare

of all spastic paraplegia cases. Causes Mutations in the PLP1 gene cause spastic paraplegia 2. The PLP1

Genetic and Rare Diseases Information Center Autosomal recessive spastic paraplegia type 20 Hereditary spastic paraplegia Patient Support and

spastic paraplegia Spastic paraparesis, childhood-onset, with distal muscle wasting Spastic paraplegia 20, autosomal recessive Spastic paraplegia, autosomal recessive, Troyer type

syndrome. More About This Health Condition Other Names for This Gene KIAA0610 SPARTIN spastic paraplegia 20 spastic paraplegia 20

with stenosis of the aqueduct of Sylvius (HSAS), MASA syndrome, spastic paraplegia type 1, and

structures when they are no longer needed. Health Conditions Related to Genetic Changes Spastic paraplegia type 4 Several hundred

Genetics provides information about Distal hereditary motor neuropathy, type V More About This Health Condition Spastic paraplegia type 31 At least

Library of Medicine) Sjögren-Larsson syndrome: MedlinePlus Genetics (National Library of Medicine) Spastic paraplegia type 5A: MedlinePlus Genetics

of Medicine) Spastic paraplegia type 31: MedlinePlus Genetics (National Library of Medicine) Spastic paraplegia type 4: MedlinePlus Genetics

optic atrophy 3 Costeff optic atrophy syndrome Infantile optic atrophy with chorea and spastic paraplegia Iraqi Jewish optic atrophy

s syndrome, see Kindler epidermolysis bullosa Kinky hair syndrome, see Menkes syndrome Kjellin syndrome, see Spastic paraplegia type 15 Kjer type

experience muscle stiffness and partial paralysis of the lower limbs (spastic paraplegia), and they

the spine ( scoliosis ). Rarely, the muscle stiffness will progress to paralysis (spastic paraplegia). Individuals with ILS cannot

OR WITHOUT ANOSMIA; HH2 HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1 KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA HYPOGONADOTROPIC HYPOGONADISM 3 WITH

and Post-Polio Syndrome Paralytic Ileus see Intestinal Obstruction Paranasal Sinus Cancer see Nasal Cancer Paraplegia see Paralysis Parasitic Diseases

see Infantile-onset ascending hereditary spastic paralysis Infantile optic atrophy with chorea and spastic paraplegia, see Costeff syndrome Infantile

progressive muscle stiffness (spasticity) and eventual paralysis of the lower limbs (paraplegia). The spasticity

TRNT1 deficiency Siegal-Cattan-Mamou disease, see Familial Mediterranean fever SIFD, see TRNT1 deficiency Silver spastic paraplegia syndrome, see Silver syndrome

Institute of Neurological Disorders and Stroke) Also in Spanish Hereditary Spastic Paraplegia (National Institute of

in Spanish Femur Shaft Fractures (Broken Thighbone) (American Academy of Orthopaedic Surgeons) Hereditary Spastic Paraplegia (National Institute of

Library of Medicine) Sjögren-Larsson syndrome: MedlinePlus Genetics (National Library of Medicine) Spastic paraplegia type 5A: MedlinePlus Genetics

Stroke) Congenital Myopathy (National Institute of Neurological Disorders and Stroke) Hereditary Spastic Paraplegia (National Institute of

see Familial glucocorticoid deficiency Hereditary ventricular hypertrophy, see Familial hypertrophic cardiomyopathy Hereditary X-linked recessive spastic paraplegia, see Spastic paraplegia type

Z X chromosome-linked sideroblastic anemia, see X-linked sideroblastic anemia X linked recessive hereditary spastic paraplegia, see Spastic paraplegia type

need joint replacement surgery. Possible Complications Complications may include: Bone fractures Deafness Deformities Heart failure Hypercalcemia Paraplegia Spinal stenosis When to

neurological disorders such as cerebral palsy (condition that causes difficulty with movement and balance), paraplegia (inability to move

over the spine Spinal cord compression Paralysis of the lower body (paraplegia) or of the

lower half of the body and both legs it is called paraplegia. If it affects both

bladder and bowel control Loss of sexual function Paralysis of limbs (paraplegia, quadriplegia) Paralysis of