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Wednesday, May 22, 2013

Cephalic Disorders - MICROCEPHALY

Article Index

  1. Cephalic Disorders
  2. ANENCEPHALY
  3. COLPOCEPHALY
  4. HOLOPROSENCEPHALY
  5. HYDRANENCEPHALY
  6. INIENCEPHALY
  7. LISSENCEPHALY
  8. MEGALENCEPHALY
  9. MICROCEPHALY
  10. PORENCEPHALY
  11. SCHIZENCEPHALY
  12. Less Common Cephalic Disorders
  13. What Research Is Being Done?
  14. Information


MICROCEPHALY is a neurological disorder in which the circumference of the head is smaller than average for the age and gender of the infant or child. Microcephaly may be congenital or it may develop in the first few years of life. The disorder may stem from a wide variety of conditions that cause abnormal growth of the brain, or from syndromes associated with chromosomal abnormalities.

Infants with microcephaly are born with either a normal or reduced head size. Subsequently the head fails to grow while the face continues to develop at a normal rate, producing a child with a small head, a large face, a receding forehead, and a loose, often wrinkled scalp. As the child grows older, the smallness of the skull becomes more obvious, although the entire body also is often underweight and dwarfed. Development of motor functions and speech may be delayed. Hyperactivity and mental retardation are common occurrences, although the degree of each varies. Convulsions may also occur. Motor ability varies, ranging from clumsiness in some to spastic quadriplegia in others.

Generally there is no specific treatment for microcephaly. Treatment is symptomatic and supportive.

In general, life expectancy for individuals with microcephaly is reduced and the prognosis for normal brain function is poor. The prognosis varies depending on the presence of associated abnormalities.

 

 

 

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