Crome syndrome

Crome syndrome
Synonyms	Cerebroretinal microangiopathy with calcifications and cysts
Pronounce	N/A
Specialty	N/A
Symptoms	Microcephaly, seizures, retinal detachment, cerebral calcifications
Complications	Developmental delay, vision loss
Onset	Infancy
Duration	Chronic
Types	N/A
Causes	Genetic mutation
Risks	Family history
Diagnosis	Clinical examination, genetic testing, imaging studies
Differential diagnosis	Aicardi syndrome, Coats disease, Sturge-Weber syndrome
Prevention	N/A
Treatment	Symptomatic treatment, seizure management, vision support
Medication	N/A
Prognosis	Variable, often progressive
Frequency	Rare
Deaths	N/A

A rare genetic disorder

Template:Medical condition (new) Crome syndrome is a rare genetic disorder characterized by a combination of ocular abnormalities, neurological symptoms, and developmental delays. It is named after the British ophthalmologist Lionel Crome, who first described the condition. The syndrome is also known as cerebroretinal syndrome.

Presentation

Individuals with Crome syndrome typically present with a range of symptoms that affect multiple systems of the body. The primary features include:

Ocular Abnormalities

- Retinal degeneration: Progressive deterioration of the retina, leading to vision impairment. - Optic atrophy: Damage to the optic nerve, resulting in vision loss. - Nystagmus: Involuntary eye movements that can affect vision.

Neurological Symptoms

- Seizures: Recurrent episodes of abnormal electrical activity in the brain. - Ataxia: Lack of voluntary coordination of muscle movements, often affecting gait and balance. - Intellectual disability: Varying degrees of cognitive impairment.

Developmental Delays

- Delayed motor milestones: Slower than normal development of motor skills such as sitting, standing, and walking. - Speech delays: Delayed development of speech and language skills.

Genetics

Crome syndrome is believed to be inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the disorder. The specific genetic mutations responsible for Crome syndrome have not been fully identified, and research is ongoing to better understand the genetic basis of the condition.

Diagnosis

Diagnosis of Crome syndrome is based on clinical evaluation, including a detailed medical history and physical examination. Ophthalmologic assessments, neurological evaluations, and genetic testing may be conducted to confirm the diagnosis and rule out other conditions with similar presentations.

Management

There is currently no cure for Crome syndrome, and treatment is primarily supportive and symptomatic. Management strategies may include: - Vision aids: Use of glasses or other visual aids to maximize remaining vision. - Seizure management: Antiepileptic medications to control seizures. - Physical therapy: To improve motor skills and coordination. - Speech therapy: To assist with communication skills.

Prognosis

The prognosis for individuals with Crome syndrome varies depending on the severity of symptoms and the presence of complications. Early intervention and supportive therapies can improve quality of life and functional outcomes for affected individuals.

Related pages

• Genetic disorder
• Retinal degeneration
• Optic atrophy
• Seizure disorder
• Developmental delay