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Charcot–Marie–Tooth disease type 1F CMT1X Charcot–Marie–Tooth disease type 1X CMT2 Charcot–Marie–Tooth disease type 2 COFS Cerebro-oculo-facio-skeletal syndrome: COLD Chronic obstructive lung disease: COPD Chronic obstructive pulmonary disease: COVID-19 Coronavirus disease 2019: CP Cerebral palsy: CP/CPPS
Generally, diseases outlined within the ICD-10 codes N00-N19, N20.0 within Chapter XIV: Diseases of the genitourinary system should be included in this category. Wikimedia Commons has media related to Kidney diseases .
Developmental disorders comprise a group of psychiatric conditions originating in childhood that involve serious impairment in different areas. There are several ways of using this term. [1] The most narrow concept is used in the category "Specific Disorders of Psychological Development" in the ICD-10. [1]
Segmental hypoplasia or Ask-Upmark kidney is a rare renal disease where a part of the kidney has undergone hypoplasia. The number of renal lobes is reduced, and the kidney size is less than two standard deviations from the average, with the weight often being over 50g in adults and 12–25g in children.
It is a genetic developmental disorder [4] with clinical diversity characterized by hypoparathyroidism, sensorineural deafness and renal disease. [5] Sensorineural deafness typically presents in childhood or adolescence. Affected people usually present with hypocalcaemia, tetany, or afebrile convulsions at any age. [1]
All people with a GFR <60 mL/min/1.73 m 2 for 3 months are defined as having chronic kidney disease. [59] Protein in the urine is regarded as an independent marker for worsening of kidney function and cardiovascular disease. Hence, British guidelines append the letter "P" to the stage of chronic kidney disease if protein loss is significant. [60]
Chronic kidney failure has numerous causes. The most common causes of chronic failure are diabetes mellitus and long-term, uncontrolled hypertension. [27] Polycystic kidney disease is another well-known cause of chronic failure. The majority of people affected with polycystic kidney disease have a family history of the disease.
The signs and symptoms of branchio-oto-renal syndrome are consistent with underdeveloped (hypoplastic) or absent kidneys with resultant chronic kidney disease or kidney failure. Ear anomalies include extra openings in front of the ears, extra pieces of skin in front of the ears (preauricular tags ), or further malformation or absence of the ...