To be
Continued
|
Children's |
Children's
Medical Centre in |
|
FACP |
Indicates
membership as a Fellow in the |
|
Idiopathic |
Of
unknown or undetermined origin, often disease-based. |
|
Paetechial
haemorrhage |
Minute,
round, nonraised haemorrhages – bleeding - into the skin or in a mucous or
serous membrane. These are the tiny red spots typically surround a spot where
someone has been hit with a fist. The same indicators are a clue to
suffocation, as well. |
|
Neonatal
Unit |
Though
Emily is in a small regional medical centre, such facilities do commonly have
neonatal units. The term neonatal refers to a child of less than one
month of age; because of their small size and lack of a mature immune system,
they are isolated and treated differently than older infants who have had all
their immunizations. In some hospitals, older infants are taken to the
Neonatal Unit if they are small for their age or if their diagnosis or
potential diagnosis is suggestive of a possible immune system dysfunction. |
|
Genetic
drift |
In
instance of “selective mating,” genetic drift is the statistical effect
resulting from the influence that chance has on the survival of variations in
genes. The effect may cause an allele and the biological trait that results
to become more common or more rare over successive generations. This has
accounted for an increase in sickle cell disorder in populations where it was
not previously observed. |
|
Tay-Sachs
Disease |
A
fatal genetic lipid storage disorder in which harmful quantities of a fatty
substance called ganglioside GM2 build up in tissues and
nerve cells in the brain. Infants with Tay-Sachs disease appear to develop
normally for the first few months of life. Then, as nerve cells become
distended with fatty material, a relentless deterioration of mental and
physical abilities occurs. The child becomes blind, deaf, and unable to
swallow. Muscles begin to atrophy and paralysis sets in. Other neurological
symptoms include dementia, seizures, and an increased startle reflex to
noise. The incidence of Tay-Sachs is particularly high among people of
Eastern European and Ashkenazi Jewish descent. Patients and carriers of
Tay-Sachs disease can be identified by a simple blood test that measures
beta-hexosaminidase A activity. Both parents must carry the mutated gene
in order to have an affected child. In these instances, there is a 25 percent
chance with each pregnancy that the child will be affected with Tay-Sachs
disease. Prenatal diagnosis is available if desired. There is no cure for
Tay-Sachs. |
|
MMR |
Measles,
Mumps, Rubella. This isn't given until the child reaches six months of age. |
|
Leukemia
vs. Leukaemia |
We
DO know how to spell, but our convention is to spell terms in the way the
SPEAKER would spell them based on his or her nationality and educational
background. The exception here is that
medical terms, most of which are Latin-based, are generically spelled the
same irrespective of nationality of the physician. |