Head Size
·
Head circumference below the 3rd centile with abnormally slow
head growth
·
Incidence: 1/1000, recurrence in
siblings 1/50
·
Causes:
o Familiar: not associated with developmental delay
o Autosomal recessive condition, associated with severe learning delay
o Congenital infection: Rubella, CMV, Toxoplasmosis, Varicella Zoster, Listeria, Syphilis
o Brain insult: eg perinatal hypoxia, neonatal meningitis. Likely to be accompanied by cerebral palsy, seizures, visual impairment, etc
o Fetal Alcohol Syndrome
·
Megalencephaly = oversized brain
· Hydrocephalus: dilated cerebrum:
o CSF
volume associated with ventricular dilatation and intraventricular
pressure
o Due to:
§ Aqueduct obstruction: injury, infection or genes
§ Arnold Chiari Malformation (downward displacement and elongation of hind
brain, with herniation into the cervical canal)
§ Acquired causes: meningeal adhesions, mass lesions, etc
·
Chronic Subdural Haematomas
·
Hydraencephaly: no cerebrum
· Benign familial anatomic megalencephaly or macrocephaly
· Metabolic Megalencephaly: late manifestation of many cerebral degenerative disorders (eg lysosomal storage diseases)
·
Neurofibromatosis
·
Cerebral Tumour
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