Triple X Syndrome - Symptoms, Causes, and Treatment

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Triple X Syndrome - Symptoms, Causes, and
Treatment

• - Specialty Care Clinics

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What is Triple X Syndrome?

• Triple X syndrome, otherwise known as trisomy
  X or 47 XXX, is a hereditary disorder that
  affects about 1 in 1,000 females. Females
  generally have two X chromosomes in all cells
  one X chromosome from per parent. A female
  suffering from triple X syndrome has three X
  chromosomes.
• Many girls and women with triple X syndrome do
  not have any symptoms or have only mild symptoms.
  In other cases, symptoms might be more apparent
  possibly including developmental delays and
  learning disabilities. Seizures and kidney
  abnormalities happen among a small number of
  girls and women suffering from triple X syndrome.
• The treatment for triple X syndrome depends upon
  what symptoms, if any, are present and their
  seriousness.

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Symptoms Of Triple X Syndrome

• Signs and symptoms could differ greatly among
  girls and women suffering from triple X syndrome.
  Many do not experience any noticeable effects or
  have only mild symptoms.
• Sometimes triple X syndrome might be related to
  these signs and symptoms
• Vertical folds of skin that cover the inside
  corners of the eyes (epicanthal folds)
• Widely spaced eyes
• Abnormally curved pinky fingers
• Flat feet
• Abnormally shaped breastbone
• Weak muscle tone (hypotonia)
• Seizures
• Kidney abnormalities

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Causes Of Triple X Syndrome

• Although triple X syndrome is genetic, it is
  generally not hereditary it is because of a
  random genetic error.
• Generally, people have forty-six chromosomes in
  each cell, organized into twenty-three pairs,
  including two sex chromosomes. One set of
  chromosomes is from the mother and another set is
  from the father. These chromosomes consist of
  genes, which carry instructions that determine
  everything from height to eye color.
• The pair of sex chromosomes either XX or XY
  decide a child's sex. A mother could give the
  child only an X chromosome, but a father could
  pass on an X or a Y chromosome
• If the child is given an X chromosome by the
  father, the XX pair makes the child genetically a
  female.
• If the child is given a Y chromosome by the
  father, the XY pair means the child is
  genetically a male.
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