Use AAPC ICD codes online conversion tool to convert ICD-9 to ICD codes for medical diagnosis coding. Stay updated on ICD coding for best. A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells. A chromosomal dysgenesis syndrome resulting from a. Free, official information about (and also ) ICDCM diagnosis code , including coding notes, detailed descriptions, index cross-references and .
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ICDCM Diagnosis Code : Melanoma of skin, site unspecified
Chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21; clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, simian crease, and moderate to severe mental retardation.
Abnormalities are variable from individual to individual and may include mental retardation, retarded growth, flat hypoplastic face with short nose, prominent epicanthic skin folds, small low-set ears with prominent antihelix, fissured and thickened tongue, laxness of joint ligaments, pelvic dysplasia, broad hands and feet, stubby fingers, transverse palmar crease, lenticular opacities and heart disease.
A disorder that results from a chromosomal abnormality. Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material either a whole chromosome or a chromosome segment.
A chromosomal abnormality consisting of the presence of a third copy of chromosome 21 in somatic cells. Typical facies with upslanting palpebral fissures is the characteristic feature of this syndrome hence the offensive designations “mongoloid idiocy” and “mongolism”.
Down syndrome is set of mental and physical symptoms that result from having an extra copy of chromosome Patients with down syndrome have an estimated 10 to fold increased risk for leukemia; most have symptoms of alzheimer’s disease by age A wide range other defects, such as congenital dodici diseases, respiratory disorders, and leukemia, may be associated.
They may have dementia.
Pathologic features include the development of neurofibrillary tangles in neurons and the deposition of amyloid beta-protein, similar to the pathology of alzheimer disease. Down syndrome occurs in approximately 1: Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, simian crease, and moderate to severe intellectual disability.
Down syndrome patients who survive into late adulthood may develop alzheimer syndrome. They may be born with heart disease.
A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome Down syndrome cannot be vodici. They may have hearing problems and problems with the intestines, eyes, thyroid and skeleton.
Usually, mental development and physical development are slower in people with down syndrome than in cocici without it. Cardiac and gastrointestinal malformations, a marked increase in the incidence of leukemia, and the early onset of alzheimer disease are also associated with ixd9 condition. A chromosomal dysgenesis syndrome resulting from a triplication or translocation of chromosome However, many people with down syndrome live productive lives well into adulthood.
Also known as trisomy 21 syndrome.
Even though people with down syndrome may have some physical and id9 features in common, symptoms of down syndrome can range from mild to severe.