This is the American ICD-10-CM version of Q98.5 - other international versions of ICD-10 Q98.5 may differ. Klinefelter's syndrome is a condition that occurs in men who have an extra x chromosome in most of their cells. Occasional abnormalities may include cryptorchidism, hypospadias, ataxia, scoliosis during adolescence, and diabetes mellitus in adulthood. Gynecomastia may be present. Boys and men with Klinefelter syndrome have one extra copy of the X chromosome, for a total of 47 chromosomes in each cell . ICD-9-CM 758.81 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.81 should only be used for claims with a date of service on or before September 30, 2015. Like 48,XXXY syndrome, Klinefelter syndrome affects male sexual development and can be associated with learning disabilities … The presence of one Y chromosome with a functioning SRY gene causes the expression of genes that determine maleness. Because of this, XXXY syndrome only affects males. Patients tend to have long legs and a slim, tall stature. The 2021 edition of ICD-10-CM Q98.5 became effective on October 1, 2020. In this context, annotation back-references refer to codes that contain: "Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA. The 48, XXYY (male) syndrome occurs 1 in 17,000 births and has traditionally been considered to be a variation of Klinefelter's syndrome. A form of male hypogonadism, characterized by the presence of an extra x chromosome, small testes, seminiferous tubule dysgenesis, elevated levels of gonadotropins, low serum testosterone, underdeveloped secondary sex characteristics, and male infertility (infertility, male). Abnormal genetic constitution in males characterized by an extra y chromosome. The presence of one Y chromosome with a functioning SRY gene causes the expression of genes that determine maleness. Gynecomastia is present in many of the patients. The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute care hospitals. Affected males are almost always effectively sterile, although advanced reproductive assistance is sometimes possible and some degree of language learning impairment may be present. Wiki May Thurner Syndrome ICD-10 Code. A sex chromosome disorder caused by the presence of an extra x chromosome in the male karyotype. The most common symptom is infertility. Genetic disease that produces sterile males with small testes lacking sperm due to xxy karyotype. A genetic disorder in males caused by having one or more extra x chromosomes. XXYY Syndrome is the name attached to the cluster of symptoms that arise as a result of the 48,XXYY chromosome pattern. Q98.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. They may be shy and have trouble fitting in.it is important to start treatment as early as possible. Often, symptoms are subtle and subjects do not realize they are affected. The 48, XXYY (male) syndrome occurs 1 in 17,000 births and has traditionally been considered to be a variation of Klinefelter's syndrome. The diagnosis codes found in the Tabular List and Alphabetic Index have been adopted under HIPAA for all healthcare settings.. Browse for your desired term or condition, or search for a specific disease / condition. In adults, possible characteristics vary widely and include little to no It can affect physical and mental development. Affected individuals are infertile and have a small penis and testes. Many experience severe acne during adolescence. Additionally, some people with this condition have recurrent seizures (epilepsy) or heart abnormalities that … Males with this disorder may have larger than normal breasts, a lack of facial and body hair, a rounded body type, and small testicles. The code is valid for the year 2020 for the submission of HIPAA-covered transactions. The primary features are infertility and small poorly functioning testicles. The syndrome can affect different stages of physical, language and social development. Sometimes, symptoms are more evident and may include weaker muscles, greater height, poor … Males typically have only two sex chromosomes, an X and a Y. Clinical Information. Klinefelter syndrome increases the risk of developing extragonadal germ cell tumors and breast cancer. Most characteristic features become evident at adolescence as hypogonadism, gynecomastia, incomplete virilization with variable eunuchoidism, and dull mentality. Dull mentality has been noted. This is the American ICD-10-CM version of Q98.4 - other international versions of ICD-10 Q98.4 may differ. 48,XXYY is one of several types of sex chromosome variations, including those that are considered as variants of Klinefelter Syndrome, 47,XXY and XXXY, XXXXY, XY/XXY and another syndrome called XYY, all of which affect males. Genetics Home Reference: 25 48,XXYY syndrome is a chromosomal condition that causes infertility, developmental and behavioral disorders, and other health problems in males. The International Classification of Diseases (ICD) is a system of universal coding that assigns uniform definitions to diagnoses. The affected individuals appear normal after birth, except for small testes. La ĉi-suba teksto estas aŭtomata traduko de la artikolo XXYY syndrome article en la angla Vikipedio, farita per la sistemo GramTrans on 2017-05-13 15:34:25. , 2015 require the use of ICD-10-CM Q98.5 became effective on October 1, 2015 require the use ICD-10-CM. 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