Cerebrovascular ferrocalcinosis


Cerebrovascular ferrocalcinosis: A condition, first described in 1930 by T. Fahr and therefore called Fahr syndrome, that is a genetic (inherited) neurological disorder characterized by abnormal deposits of calcium in certain of areas of the brain (including the basal ganglia and the cerebral cortex).

Symptoms may include motor function deterioration, dementia, mental retardation, spastic paralysis, dysarthria (poorly articulated speech), spasticity (stiffness of the limbs), ocular (eye) problems, and athetosis (involuntary, writhing movements).

Features of Parkinson’s disease such as tremors, rigidity (resistance to imposed movement), a mask-like facial appearance, shuffling gait, and a “pill-rolling” motion of the fingers may also occur in individuals with Fahr’s syndrome. Other symptoms may include dystonia (disordered muscle tone), chorea (involuntary, rapid, jerky movements), and seizures. Onset of the disorder may occur at any time from childhood to adulthood.

Fahr syndrome thus involves abnormalities of the neurologic system (cerebral calcification, dementia, spastic paraplegia, athetosis), skull (microcephaly, i.e. an abnormally small head), eyes (glaucoma, optic nerve atrophy, retinitis pigmentosa), and, we would add, a significant hormone problem, namely hypoparathyroidism (the parathyroid gland regulates calcium).

The disease is inherited as an autosomal recessive trait in which both parents carry a Fahr gene and each of their children (boys and girls alike) stands a 1 on 4 (25%) risk of receiving both Fahr genes and therefore having this dread disease.

There is no cure for Fahr’s syndrome, nor is there a standard course of treatment. Treatment is directed toward minimizing symptoms.

The prognosis (outlook) for individuals with Fahr’s syndrome is poor. Progressive neurological deterioration generally results in disability and death.

Alternative names for this syndrome include, nonarteriosclerotic cerebral calcification, striopallidodentate calcinosis, and SPD calcinosis.

Read Also:

  • Cerebrum

    Cerebrum: The largest part of the brain. It is divided into two hemispheres, or halves. The word “cerebrum” is the Latin word for “brain.” The Romans used the same word to refer to the “skull” (which houses the brain) and the “head” (which houses the skull). And in Rome “cerebrum” also meant “understanding” (and a […]

  • Certified nurse-midwife

    Certified nurse-midwife: A person with an AS, BS, or Master’s degree in nursing who has also completed specialized training in midwifery. In the US, certified nurse-midwives (CNMs) must earn certification from the American College of Nurse-Midwives.

  • Certified midwife

    Certified midwife: A midwife who has been certified by her state or national agency for credentialing midwives.

  • Certified professional midwife

    Certified professional midwife: A midwife who has completed a degree in midwifery at a credentialed educational institution. Abbreviated CPM.

  • Ceruloplasmin deficiency

    Ceruloplasmin deficiency: A genetic disorder that is due to a lack of ceruloplasmin, a protein that is involved in iron transport. The absence of ceruloplasmin leads to the abnormal deposition of iron in the pancreas (causing diabetes), liver (causing cirrhosis), retina (damaging vision), and brain (causing dementia and Parkinson’s disease). Aggressive treatment with deferoxamine, a […]


Disclaimer: Cerebrovascular ferrocalcinosis definition / meaning should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional. All content on this website is for informational purposes only.