Septo-optic dysplasia

Septo-optic dysplasia

Neurology

Neurology

Stroke: Clinical
Seizures: Clinical
Headaches: Clinical
Dizziness and vertigo: Clinical
Hyperkinetic movement disorders: Clinical
Hypokinetic movement disorders: Clinical
Muscle weakness: Clinical
Disorders of consciousness: Clinical
Brain tumors: Clinical
Meningitis, encephalitis and brain abscesses: Clinical
Lower back pain: Clinical
Spinal cord disorders: Pathology review
Traumatic brain injury: Clinical
Dementia: Pathology review
Spina bifida
Chiari malformation
Dandy-Walker malformation
Syringomyelia
Tethered spinal cord syndrome
Aqueductal stenosis
Septo-optic dysplasia
Cerebral palsy
Spinocerebellar ataxia (NORD)
Transient ischemic attack
Ischemic stroke
Intracerebral hemorrhage
Epidural hematoma
Subdural hematoma
Subarachnoid hemorrhage
Saccular aneurysm
Arteriovenous malformation
Broca aphasia
Wernicke aphasia
Wernicke-Korsakoff syndrome
Kluver-Bucy syndrome
Concussion and traumatic brain injury
Shaken baby syndrome
Seizures and epilepsy
Febrile seizure
Early infantile epileptic encephalopathy (NORD)
Tension headache
Cluster headache
Migraine
Idiopathic intracranial hypertension
Trigeminal neuralgia
Cavernous sinus thrombosis
Alzheimer disease
Vascular dementia
Frontotemporal dementia
Dementia with Lewy bodies
Creutzfeldt-Jakob disease
Normal pressure hydrocephalus
Torticollis
Essential tremor
Restless legs syndrome
Parkinson disease
Huntington disease
Opsoclonus myoclonus syndrome (NORD)
Multiple sclerosis
Central pontine myelinolysis
Acute disseminated encephalomyelitis
Transverse myelitis
JC virus (Progressive multifocal leukoencephalopathy)
Adult brain tumors
Acoustic neuroma (schwannoma)
Pituitary adenoma
Pediatric brain tumors
Brain herniation
Brown-Sequard Syndrome
Cauda equina syndrome
Treponema pallidum (Syphilis)
Vitamin B12 deficiency
Friedreich ataxia
Neurogenic bladder
Meningitis
Neonatal meningitis
Encephalitis
Brain abscess
Epidural abscess

Flashcards

Septo-optic dysplasia

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Key Takeaways

Septo-optic dysplasia (SOD), also known as de Morsier syndrome, is a rare congenital malformation syndrome featuring underdevelopment of the optic nerve that leads to blindness or visual impairment; pituitary gland dysfunction that causes various hormonal deficiencies; and absence of the septum pellucidum, a thin membrane that separates the brain's lateral ventricles. Symptoms include nystagmus, visual impairment, seizures, short stature due to growth hormone deficiency, diabetes insipidus due to vasopressin deficiency, and hyperbilirubinemia. There is no cure for SOD, but various treatments and therapies can help manage its symptoms, including hormone replacement therapy, special education, and rehabilitation services.