Hereditary Spastic Paraplegia 23 (SPG23)

Alias:

Spastic Paraplegia 23

Spastic Paraparesis-Vitiligo-Premature Graying-Characteristic Facies Syndrome

Spastic Paraplegia with Pigmentary Abnormalities

Lison Syndrome

Spg23

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hereditary Spastic Paraplegia 23, also known as spastic paraplegia 23, is related to hereditary spastic paraplegia and spastic paraplegia 23, autosomal recessive. An important gene associated with Hereditary Spastic Paraplegia 23 is DSTYK (Dual Serine/Threonine And Tyrosine Protein Kinase). Related phenotypes are hyperreflexia and intellectual disability, mild

Related ID：

MALACARDS：HRD210