Paraphrase the following paragraph Diagnosing Marfan syndrome: Diagnosing a person with Marfan syndrome is difficult bec
Posted: Tue May 17, 2022 3:07 pm
Paraphrase the following paragraph
Diagnosing Marfan syndrome:
Diagnosing a person with Marfan syndrome is difficult because
the symptoms and the signs can vary from one person to the other.
However, in most situations, a diagnosis will be based on a
thorough physical examination followed by a detailed assessment of
a person’s medical and family history. The physical examinations
that the Doctor will carry out should include, listening to a
patient’s heart, checking the skin for stretch marks, and looking
for any physical features of the syndrome, like a high palate,
curvature of the spine, and long or thin arms and legs. Marfan
syndrome can be especially difficult to diagnose in children
because most of the signs and symptoms do not usually appear until
later in childhood and teenage years. Although it is rare to
diagnose a child with Marfan syndrome if the child is suspected to
have the syndrome the Doctors would carefully monitor the condition
of the child to detect any developing symptoms and treat them as
soon as possible. Since Marfan syndrome may be difficult to
diagnose, the geneticist in charge of diagnosing the patient may
compare the signs and symptoms against the Ghent criteria. The
Ghent criteria is a diagnostic checklist, that consists of major
and minor criteria, that enable geneticists and other healthcare
professionals to tell the difference between Marfan syndrome and
any other similar syndromes. The major criteria, which may include
an enlarged aorta or a tear in the aorta, dislocation of the lens
of the eye, or at least four skeletal problems, such as flat feet
or scoliosis, are certain features or symptoms that are common
within people who have Marfan syndrome, however, are rare in people
who don’t have it. The minor criteria, on the other hand, which may
include short-sightedness, unexplained stretch marks, and loose
joints, are certain features and symptoms present in people with
Marfan syndrome but are also present in people who don’t have the
syndrome. If the patient has a family history of Marfan syndrome,
for example, then that person needs to be diagnosed with one of the
conditions found in the major criteria and one of the minor
criteria, however, if the patient doesn’t have a history of Marfan
syndrome, then they’ll need to be diagnosed with two of the
conditions found in the major criteria and one of the conditions
found in the minor criteria. To use the Ghent criteria to be
diagnosed with Marfan syndrome, the patient must have several
different symptoms so another way to diagnose this syndrome would
be to perform a blood test. This blood test looks for changes in
the FBN1 gene (Unknown, 2022).
Diagnosing Marfan syndrome:
Diagnosing a person with Marfan syndrome is difficult because
the symptoms and the signs can vary from one person to the other.
However, in most situations, a diagnosis will be based on a
thorough physical examination followed by a detailed assessment of
a person’s medical and family history. The physical examinations
that the Doctor will carry out should include, listening to a
patient’s heart, checking the skin for stretch marks, and looking
for any physical features of the syndrome, like a high palate,
curvature of the spine, and long or thin arms and legs. Marfan
syndrome can be especially difficult to diagnose in children
because most of the signs and symptoms do not usually appear until
later in childhood and teenage years. Although it is rare to
diagnose a child with Marfan syndrome if the child is suspected to
have the syndrome the Doctors would carefully monitor the condition
of the child to detect any developing symptoms and treat them as
soon as possible. Since Marfan syndrome may be difficult to
diagnose, the geneticist in charge of diagnosing the patient may
compare the signs and symptoms against the Ghent criteria. The
Ghent criteria is a diagnostic checklist, that consists of major
and minor criteria, that enable geneticists and other healthcare
professionals to tell the difference between Marfan syndrome and
any other similar syndromes. The major criteria, which may include
an enlarged aorta or a tear in the aorta, dislocation of the lens
of the eye, or at least four skeletal problems, such as flat feet
or scoliosis, are certain features or symptoms that are common
within people who have Marfan syndrome, however, are rare in people
who don’t have it. The minor criteria, on the other hand, which may
include short-sightedness, unexplained stretch marks, and loose
joints, are certain features and symptoms present in people with
Marfan syndrome but are also present in people who don’t have the
syndrome. If the patient has a family history of Marfan syndrome,
for example, then that person needs to be diagnosed with one of the
conditions found in the major criteria and one of the minor
criteria, however, if the patient doesn’t have a history of Marfan
syndrome, then they’ll need to be diagnosed with two of the
conditions found in the major criteria and one of the conditions
found in the minor criteria. To use the Ghent criteria to be
diagnosed with Marfan syndrome, the patient must have several
different symptoms so another way to diagnose this syndrome would
be to perform a blood test. This blood test looks for changes in
the FBN1 gene (Unknown, 2022).