Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome

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Definition

A rare neurometabolic disorder due to serine deficiency characterized by neonatal to infantile onset of global developmental delay, postnatal microcephaly and intellectual disability, which may be associated with slowly progressive spastic tetraplegia mainly affecting the lower extremities, seizures, and brain MRI findings including thin corpus callosum, delayed myelination and cerebral atrophy. Additional symptoms include brisk deep tendon reflexes, extensor plantar responses, behavioral abnormalities (such as irritability, hyperactivity, sleep disorder), abnormal hand movements and stereotypy.

NIH genetic and rare disease info

Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome is a rare disease.

Rare and genetic diseases

Rare diseases - Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome

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Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome

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