Turner syndrome
Turner syndrome is a chromosomal condition that alters development in females. Women with this condition tend to be shorter than average and are usually unable to conceive a child (infertile) because of an absence of ovarian function. Other features of this condition that can vary among women who have Turner syndrome include: extra skin on the ...
Turner syndrome is not considered a disability, although it can cause certain learning challenges, including with learning mathematics and with memory. 7 Most girls and women with Turner syndrome lead normal, healthy, productive lives with proper medical care. My daughter has been diagnosed with Turner syndrome.
The heart defects associated with some cases of Turner syndrome can increase the risk of severe, life-threatening complications including high blood pressure of the arteries of the lungs (pulmonary hypertension) or aortic dissection, a condition in which there is a tear in the inner wall of the aorta.
Turner's syndrome, unspecified Q96. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM Q96. 9 became effective on October 1, 2021.
Turner syndrome is a genetic disorder affecting girls and women. The cause of Turner syndrome is a completely or partially missing X chromosome. Turner syndrome symptoms include short stature and lack of breast development and periods. Treatment for Turner syndrome may include hormone therapy.
Other names for Turner's syndrome include monosomy X, 45X and Ullrich-Turner syndrome.
Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic condition in which a female is partially or completely missing an X chromosome. Signs and symptoms vary among those affected.
Turner syndrome is caused by partial or complete loss (monosomy) of the second sex chromosome. Chromosomes are found in the nucleus of all body cells. They carry the genetic characteristics of each individual and they come in pairs. We receive one copy from each parent.
Karyotyping. Karyotyping is a test that involves analysing the 23 pairs of chromosomes. It's often used when Turner syndrome is suspected. The test can either be carried out while the baby is inside the womb – by taking a sample of amniotic fluid (amniocentesis) – or after birth by taking a sample of the baby's blood.
Turner syndrome is a female-only genetic disorder that affects about 1 in every 2,000 baby girls. A girl with Turner syndrome only has 1 normal X sex chromosome, rather than the usual 2. This chromosome variation happens randomly when the baby is conceived in the womb.
Appearance. Features of Turner syndrome may include a short neck with a webbed appearance, low hairline at the back of the neck, low-set ears, hands and feet that are swollen or puffy at birth, and soft nails that turn upward. Stature. Girls with Turner syndrome grow more slowly than other children.
Monosomy X, or Turner syndrome, occurs when a baby is born with only one X sex chromosome, rather than the usual pair (either two Xs or one X and one Y sex chromosome).
Definition. XO syndrome is a disorder of the sex chromosomes, occurring in females, in which one of the two X chromosomes is completely or partially absent. XO syndrome causes a number of symptoms that vary greatly among individuals, but generally include small stature, amennorhea and infertility.
iii) Turner's syndrome is a condition in which the female is born with only one copy of the X-chromosome. The karyotype will be 44 A + X.
Turner syndrome is associated with a 45,X karyotype, with a single X chromosome. Mosaicism is not uncommon, however, with a separate cell line containing either a normal 46,XX or XY karyotype, or 46 chromosomes including a structurally rearranged X or Y.
Turner syndrome is a genetic disorder that affects a girl's development. The cause is a missing or incomplete x chromosome. Girls who have it are short, and their ovaries don't work properly. Most are infertile. They are at risk for health difficulties such as high blood pressure, kidney problems, diabetes, cataracts, osteoporosis and thyroid problems.other physical features typical of turner syndrome are#N#short, "webbed" neck with folds of skin from tops of shoulders to sides of neck#N#low hairline in the back#N#low-set ears#N#swollen hands and feet#N#there is no cure for turner syndrome, but there are some treatments for the symptoms. Growth hormone often helps girls reach heights that are close to average. Hormone replacement can stimulate sexual development. Assisted reproduction techniques can help some women with turner syndrome get pregnant. nih: national institute of child health and human development 1 short, "webbed" neck with folds of skin from tops of shoulders to sides of neck 2 low hairline in the back 3 low-set ears 4 swollen hands and feet
They are at risk for health difficulties such as high blood pressure, kidney problems, diabetes, cataracts, osteoporosis and thyroid problems.other physical features typical of turner syndrome are. short, "webbed" neck with folds of skin from tops of shoulders to sides of neck. low hairline in the back. low-set ears.
A gonadal dysgenesis syndrome occurring in phenotypic females, characterized by the absence of a part or all of one of the sex chromosomes. Signs and symptoms include short stature, webbing of neck, low-set ears, hypogonadism, and sterility. A gonadal dysgenesis syndrome occurring in phenotypic females, characterized by the complete absence ...
Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example when having 45 or 47 chromosomes when 46 is expected in a human cell. It does not include a difference of one or more complete sets of chromosomes, which is called euploidy.
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q96. Click on any term below to browse the alphabetical index.
Code is only used for female patients. Q96.9 is a billable ICD code used to specify a diagnosis of turner's syndrome, unspecified. A 'billable code' is detailed enough to be used to specify a medical diagnosis. Documentation insufficient to determine if the condition was present at the time of inpatient admission.
The ICD code Q96 is used to code Aneuploidy. Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example when having 45 or 47 chromosomes when 46 is expected in a human cell. It does not include a difference of one or more complete sets of chromosomes, which is called euploidy. An extra or missing chromosome is ...
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis. The Center for Medicare & Medicaid Services (CMS) requires medical coders to indicate whether or not a condition was present at the time of admission, in order to properly assign MS-DRG codes.