If the gene defect(s) are expressed during fetal development, the condition is present at birth. This is the congenital form of the disorder
As microcephaly is often associated with chromosomal abnormalities, the specific genetic cause for a person's microcephaly should be determined, if possible. Genetic counseling is available to help parents
Other possible causes of microcephaly include infections during pregnancy (rubella, cytomegalovirus, toxoplasmosis), adverse effects of medication, and the excessive use of alcohol by the mother during pregnancy
Genetic diseases are called heredity diseases . They may be congenital or may appear later on eh hare lip , microcephaly etc.
Head circumference is a direct reflection of head growth When the growth is below norms it is classed as microcephaly. The result of microcephaly is a degree of retardation in growth. If the microcephaly is benign, the limitation is not significant in development.
Microcephaly is a rare neurological condition and occurs worldwide. Little detailed information on the prevalence of the disorder is available. Microcephaly does not appear to be more prevalent among any race or one gender
the base sequences signify what genetic code
Microcephaly is an extremely rare condition in which the fetus's head circumference is lower then one percentile.
Scientists made skull casts of modern individuals with microcephaly to study the physical characteristics and differences in skull shape compared to normal individuals. By examining these casts, researchers can better understand the condition of microcephaly and how it affects the development of the skull. This research can also help in diagnosing and distinguishing microcephaly from other cranial abnormalities.
It is a direct - and exact - copy of the Genetic Sequence of the Dna; except that the base Thymine in Dna is replaced by the base Uracil in Rna.
they live to be 20 or to aleast 35 if they are lucky
This is quite rare but I have nursed one. The diagnosis is made usually by identifying the abnormal signs of the infant. It is confirmed by skull x-ray (microcephaly) and genetic testing (abnormal chrosome 5). Treatment is symptomatic, there is no cure.
The damage from microcephaly comes because of the cramped interior of the skull. This lack of space exerts pressure on the growing brain. This causes impairment and delayed development of functions such as speech and control of muscles