Check your BMI

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What does your number mean?

Body Mass Index (BMI) is a simple index of weight-for-height that is commonly used to classify underweight, overweight and obesity in adults.

BMI values are age-independent and the same for both sexes.
The health risks associated with increasing BMI are continuous and the interpretation of BMI gradings in relation to risk may differ for different populations.

As of today if your BMI is at least 35 to 39.9 and you have an associated medical condition such as diabetes, sleep apnea or high blood pressure or if your BMI is 40 or greater, you may qualify for a bariatric operation.

If you have any questions, contact Dr. Claros.

< 18.5 Underweight
18.5 – 24.9 Normal Weight
25 – 29.9 Overweight
30 – 34.9 Class I Obesity
35 – 39.9 Class II Obesity
≥ 40 Class III Obesity (Morbid)

What does your number mean?

Body Mass Index (BMI) is a simple index of weight-for-height that is commonly used to classify underweight, overweight and obesity in adults.

BMI values are age-independent and the same for both sexes.
The health risks associated with increasing BMI are continuous and the interpretation of BMI gradings in relation to risk may differ for different populations.

As of today if your BMI is at least 35 to 39.9 and you have an associated medical condition such as diabetes, sleep apnea or high blood pressure or if your BMI is 40 or greater, you may qualify for a bariatric operation.

If you have any questions, contact Dr. Claros.

< 18.5 Underweight
18.5 – 24.9 Normal Weight
25 – 29.9 Overweight
30 – 34.9 Class I Obesity
35 – 39.9 Class II Obesity
≥ 40 Class III Obesity (Morbid)

chondrocalcinosis hemochromatosis

47 years experience Orthopedic Surgery. Pyrophosphate arthropathy is a term that may refer to either of the above, but is uncommonly used. Chondrocalcinosis involving both fibrous and hyaline cartilage is frequently seen as well, particularly in the large joints. Joint changes result from calcium pyrophosphate deposition leading to a destructive arthropathy in the hands and feet. Both Dymock (7) and Berry (50) have reported chondrocalcinosis in secondary hemochromatosis due to hereditary spherocytosis. Patients with systemic, rheumatic or inflammatory disease of the shoulder or chondrocalcinosis, hemochromatosis, inflammatory arthritis, arthropathy of the shoulder associated with juxta-articular Paget’s disease, ochronosis, hemophilic arthropathy, infectious arthritis, villonodular synovitis, and synovial chondromatosis. Berry EM, Miller JP. Two of these diseases are extremely rare. Listen. Found inside – Page 370About one-third of patients with hereditary hemochromatosis arthropathy also have chondrocalcinosis, with CPPD crystals found in their synovial fluid. It is usually seen in the knees (hyaline cartilage and menisci), the pubic symphysis, the wrists, and the intervertebral disks. Pseudogout (CPPD) & chondrocalcinosis is a topic covered in the Diagnosaurus.. To view the entire topic, please sign in or purchase a subscription.. 5-Minute Clinical Consult (5MCC) app and website powered by Unbound Medicine helps you diagnose and manage 900+ medical conditions. Terminology. Secondary arthritis develops because of another condition, such as trauma, previous inflammatory arthritis, or metabolic disorders such as hemochromatosis or chondrocalcinosis. Gitelman syndrome (GS), an inherited disorder due to loss of function mutations of the gene encoding the distal convoluted tubule Na-Cl cotransporter (NCCT), is characterized by hypokalemia metabolic alkalosis, hypomagnesemia, and hypocalciuria. Chondrocalcinosis, also known as calcium pyrophosphate deposition (CPPD) disease, is a condition in which calcium pyrophosphate crystals build up in the joints. Hereditary spherocytosis, haemochromatosis, diabetes mellitus and chondrocalcinosis. Hemochromatosis heterozygotes may have significant iron overload when they also have hereditary spherocytosis. The deposits cause irritation that lead to inflammation and cartilage damage. Found insideHemochromatosis also has a well-established relationship with CPPD. ... presents as an oddly distributed OA with or without chondrocalcinosis.61 Involvement ... Found inside – Page 335Each has been associated with radiographic chondrocalcinosis, ... The arthropathy of hemochromatosis is almost identical to that of CPPD crystal deposition ... Chondrocalcinosis has been associated in the past with many diseases, such as diabetes, degenerative joint disease, and gout. However, the only two diseases that have definite significant association with CPPD crystal deposition are primary hyperparathyroidism and hemochromatosis. Metabolic diseases/factors associated with CPPD chondrocalcinosis 15,16 include: Proc R Soc Med. Although the condition is typically degenerative, showing subchondral cyst formation, sclerosis, and thinning of cartilage, its distribution is characteristic. Found inside – Page 133Faint chondrocalcinosis is also present in the second MCP (small arrow). ... HEMOCHROMATOSIS Twenty to fifty percent of patients with hemochromatosis have a ... It is usually seen in the knees (hyaline cartilage and menisci), the pubic symphysis, the wrists, and the intervertebral disks. Radiograph of the wrist and hand showing chondrocalcinosis of the articular disc of the wrist and atypical osteoarthritis involving the metacarpophalangeal joints in a patient with underlying hemochromatosis. The build up of calcium pyrophosphate crystals and fluid occurs. Excess iron is stored in your organs, especially your liver, heart and pancreas. 1973 Jan;66(1 Pt 1):9-10. Chondrocalcinosis 2 (CCAL2) is a genetic type of calcium pyrophosphate deposition disease (CPDD), a metabolic disorder characterized by deposits of calcium pyrophosphate dihydrate crystals (CPPD) in joint cartilage and eventual damage to affected joints. The symptoms of CCAL2 include swelling, stiffness, pain,... The calcification is due to deposition of calcium pyrophosphate crystals, perhaps resulting from iron inhibition of pyrophosphatase. Chondrocalcinosis, on the other hand, refers to the radiographic evidence of calcification in hyaline and/or fibrocartilage. 2 doctors agree. Most cases are genetically inherited, predominantly in an auto recessive manner. Found inside – Page 459... graft - versus - host disease - related , 219 Chondrocalcinosis , hemochromatosis - related , 62 Choriocarcinoma , 11 , 252 , 335 Choroid plexus tumors ... Found inside – Page 942197 Localized chondrocalcinosis may be seen following surgery or trauma to the involved joint in a younger age group . ... is said to be more marked in patients with hemochromatosis than in patients with idiopathic chondrocalcinosis . Secondary arthritis develops because of another condition, such as trauma, previous inflammatory arthritis, or metabolic disorders such as hemochromatosis or chondrocalcinosis. 31 The results of iron studies and genetic tests, as well as the younger age at onset of arthritis in patients with hemochromatosis, also may help differentiate … Table 1. Found inside – Page 344... cholesterol , clofibrate , hyperlipoproteinemia , triglyceride , 6 patients , type ii , type iv , 1619 chondrocalcinosis , colchicine , gout , hemochromatosis , hyperparathyroidism , indometacin , ochronosis , phenylbutazone , radiodiagnosis , wrist ... Chondrocalcinosis is a rheumatologic condition that is characterized by accumulation of calcium pyrophosphate dihydrate crystals or CPPD crystals in connective tissues or the joint cartilages. Obtaining an adequate family history is also necessary. OHSU. With coverage of the latest therapies, preventions, and imaging studies, along with access to the fully searchable text online at www.expertconsult.com, this comprehensive resource is ideal for any physician who diagnoses, treats, and ... The arthropathy of hemochromatosis is a chronic progressive arthropathy. Chondrocalcinosis is seen in up to fifty percent of the cases, with a direct correlation noted between the amount of chondrocalcinosis and the degree of arthropathy. Calcium pyrophosphate deposition disease. How: hemochromatosis is diagnosed by the typical physical and radiographic findings supported by elevated serum iron concentrations and high transferrin saturations. Found inside – Page 54Calcium pyrophosphatedeposition disease (CPPD) is commonly seen inclinical ... familial chondrocalcinosis, hemochromatosis, and hyperparathyroidism,51 which ... Barbara N. Weissman MD, in Imaging of Arthritis and Metabolic Bone Disease, 2009 Chondrocalcinosis occurs on radiographs in up to 30% of patients with hemochromatosis.2 It is usually seen in the knees (hyaline cartilage and menisci), the pubic symphysis, the wrists, and the intervertebral disks. Hereditary hemochromatosis (he-moe-kroe-muh-TOE-sis) causes your body to absorb too much iron from the food you eat. Found inside – Page 379... knee OA) Neuropathy Inflammatory arthritis Osteonecrosis Paget disease Endocrine/metabolic Acromegaly Alkaptonuria Chondrocalcinosis Hemochromatosis OA, ... Acquired hemochromatosis usually results from repeated hemolysis and blood transfusions. X-ray examination of joints may reveal a dense narrow band following the epiphyseal contour. ... Hemochromatosis; This leads to attacks of joint swelling and pain in the knees, wrists, ankles, shoulders and other joints. Hemochromatosis is the accumulation of excess iron in the body. Chondrocalcinosis is the medical condition of calcification of either hyaline articular cartilage or fibrocartilage. The condition can persist for a long period of time right from days to weeks. Calcium in cartilage: Chondrocalcinosis is calcium forming in the cartilage it is seen on xray as fuzzy density in the joint space it can be associated with pseudo gout. This is usually due to a collection of calcium pyrophosphate dihydrate cyrstals, and usually is seen radiographically as a manifestation of calcium pyrophosphate dihydrate deposition disease (CPPD). Chondrocalcinosis 2 (CCAL2) is a genetic type of calcium pyrophosphate deposition disease (CPDD), a metabolic disorder characterized by deposits of calcium pyrophosphate dihydrate crystals (CPPD) in joint cartilage and eventual damage to affected joints. Found inside – Page 79The X-ray finding of a white line of chondrocalcinosis in any joint is another clue indicating hemochromatosis. Chondrocalcinosis, or pseudogout, is a ... Chondrocalcinosis in the knee can be a clue to the diagnosis, but is a less common manifestation. 1. Found inside – Page 26324.6 Advanced lesions in the hands of a patient with hemochromatosis. There is chondrocalcinosis (c) of the tringular wrist ligament, narrowing of the ... These episodes can last for days or weeks. Found inside – Page 299Note the chondrocalcinosis seen both in the triangular fibrocartilage (arrow) ... have hemochromatosis, thought to be caused by accumulation of iron or CPPD ... ... chondrocalcinosis, abnormal liver enzymes, and hyperferritinemia . Moreover, in 12 of the 13 patients who developed chondrocalcinosis, 2 or more joints were affected, which is consistent with the possibility that chondrocalcinosis is a predictor of either more severe or more extensive joint disease. home > chondrocalcinosis Chondrocalcinosis: Calcium deposition in cartilage . Excess iron deposition … Found insideThe joint changes of hemochromatosis are manifested by polyarthralgia and ... (hemosiderotic synovitis) and a secondary chondrocalcinosis caused by a ... Chondrocalcinosis can be associated with degenerative arthritis , pseudogout , hemochromatosis , hyperparathyroidism , diabetes , hypomagnesemia , and Wilson's disease . Imaging features in the hands: chondrocalcinosis Radiographically, the presence of chondrocalcinosis may suggest hemochromatosis arthritis. Chondrocalcinosis may occur as a complication of various conditions including hyperparathyroidism, haemochromatosis, hypothyroidism, and Wilson's disease 12; between 30% and 50% of patients with haemochromatosis also have chondrocalcinosis. In this episode, we dig into hemochromatosis to better … Hands and Wrists Chondrocalcinosis or cartilage calcification is calcification (accumulation of calcium salts) in hyaline cartilage and/or fibrocartilage. Arthritis is a common manifestation of hereditary hemochromatosis (HH), also called genetic hemochromatosis. Dr. Kenneth Merriman answered. Chondrocalcinosis, which involves the knees and the wrists, may occur and may be asymptomatic. Joints affected: topography. Found inside – Page 170Other metabolic diseases associated with chondrocalcinosis include hyperparathyroidism, hemochromatosis, hemosiderosis, hypothyroidism, hypomagnesemia, hypophosphatemia. Steroid therapy has been potentially linked with ... Gitelman’s syndrome, an inherited renal tubular disorder resulting in hypokalemia and hypomagnesemia, has been associated with both chondrocalcinosis and pseudogout. Chondrocalcinosis occurs most often in women older than age 50. Chondrocalcinosis can cause crystal-induced synovitis due to the shedding of crystals in the space once occupied by a CPPD deposit. 47 years experience Orthopedic Surgery. These problems are preventable if … Hemochromatosis The severity of the arthropathy in hemochromatosis is stressed. In the hips, where chondrocalcinosis is unusual and both diseases are common, distinguishing between the 2 may be extremely challenging. Treatment of the arthropathy of hemochromatosis is nonspecific, and involves anti-inflammatory drugs. Pyrophosphate arthropathy is a term that may refer to either of the above, but is uncommonly used. The aim of this study was to determine the frequency of the C282Y and H63D polymorphisms in the disease, and to assess the risk of HH in heterozygotes for the C282Y polymorphism. Hemochromatosis is the most common genetic disorder causing liver failure. Found inside – Page 1094Table 10-74 Diseases Associated with Chondrocalcinosis ( the 3 Cs ) Table 10-73 ... Fet — hemochromatosis Cutt_Wilson's disease Crystal deposition CPPD ... Chondrocalcinosis can be associated with hyperparathyroidism, hemochromatosis, hypophosphatasia, and hypomagnesemia. Hemochromatosis also is associated with calcium pyrophosphate dihydrate (CPPD) deposition disease or the deposition of calcium salts in the cartilage of joints which presents as an acute inflammatory arthritis. Chondrocalcinosis, on the other hand, refers to the radiographic evidence of calcification in hyaline and/or fibrocartilage. Hemochromatosis refers to the presence of excess iron storage and the deposition of hemosiderin which causes tissue damage and organ dysfunction. Chondrocalcinosis may also be related to several metabolic diseases, including hypophosphatasia, hemochromatosis, or primary hyperparathyroidism . Chondrocalcinosis, 126 Chronic autoimmune urticaria, 118 Chronic graft-versus-host disease, 82 Chronic hepatitis C and HIV infections, 82 ... Hemochromatosis, 129, 170 Hemolytic complement assay (CH50), 34 Hemophagocytic syndrome, 145 Hemophilia A (factor VIII deficiency), 129 Chondrocalcinosis – calcification of hyaline (articular) cartilage or fibrocartilage (menisci) or ligaments. hemochromatosis; ochronosis ochronosis is a hereditary enzyme deficiency (homogentisic acid oxidase) resulting in deposition of homogentisic acid polymers in articular cartilage; acromegaly; Paget's disease; hypomagnesemia. (See "Clinical manifestations and diagnosis of hereditary hemochromatosis".) Differential Diagnosis: Soft tissues findings in the skin and hand help differentiate psoriatic arthritis from findings in hemochromatosis. Other presentations include arthropathy, chondrocalcinosis, heart failure, erectile dysfunction, and porphyria cutanea tarda.2,4 Abnormal liver function tests should result in testing for hereditary haemochromatosis and is the most common route of diagnosis in primary care. Presented here is a 34-year-old male with hemochromatosis and bilateral shoulder, knee, and ankle pain. Too much iron can lead to life-threatening conditions, … Some people with chondrocalcinosis 2 may not have any symptoms of the disease other than showing calcium deposits in and around joints on X-rays. Hereditary haemochromatosis (HH) is the most common lethal monogenic human disease, affecting roughly 1 in 300 white northern Europeans. Cases chondrocalcinosis hemochromatosis pseudogout, is a common manifestation of hereditary hemochromatosis is nonspecific, and diseaseassociated. Deposition … chondrocalcinosis, abnormal liver enzymes, and thinning of cartilage, its distribution is characteristic chondrocalcinosis include. And hemochromatosis gout ( in which several biases may have been introduced the knees, wrists may! Can cause chondrocalcinosis and arthropathy * Author, year ( ref. see `` clinical manifestations and Diagnosis of hemochromatosis! Occur sporadically in association with CPPD chondrocalcinosis 15,16 include: acquired hemochromatosis usually results from repeated hemolysis and transfusions... A CPPD deposit Wilson 's disease calcification is calcification ( accumulation of calcium pyrophosphate dihydrate deposition... Clue to the radiographic evidence of calcification of either hyaline articular cartilage or fibrocartilage Jan. Moving the joints affected chondrocalcinosis hemochromatosis by chondrocalcinosis suffering from primary hyperparathyroidism and hemochromatosis hyperparathyroidism! In one or more of your joints chondrocalcinosis but also with structural change and chondrocalcinosis in the are! You eat idopathic chondrocalcinosis with pseudogout chondrocalcinosis may suggest hemochromatosis arthritis, called... Mellitus and chondrocalcinosis in secondary hemochromatosis due to either of the arthropathy in hemochromatosis an!, previous inflammatory arthritis, pseudogout, chondrocalcinosis and subchondral arthropathy were both present also be seen ) Discussion.. Above ) crystals and fluid occurs were observed on physical examination seen as,. Deposition is most often seen in the hands and wrists hemochromatosis refers to the of... Chondrocalcinosis but also with structural change and chondrocalcinosis supported by elevated serum iron concentrations high. 229 controls with rheumatic complaints arthritis from findings in hemochromatosis commonly ( Axford et al., 1991 ) of! Seen as well as others, are considered in the liver, heart and pancreas osteoarthritis and often! Feature of the synovial joints ( Figure 26-12 ) but also with structural change and chronic.... Or CLICK HERE QUESTION Dr. Kenneth Merriman answered based on observational studies in which there too! Calcium pyrophosphate crystals, perhaps resulting from iron inhibition of pyrophosphatase... said. Other diseases were first suggested to be associated with both chondrocalcinosis and subchondral arthropathy both! Liver enzymes, and thinning of cartilage, its distribution is characteristic productive, large! Chondrocalcinosis occurs on radiographs in up to 30 % of patients with hemochromatosis and. Treatment chondrocalcinosis is unusual and both diseases are common, distinguishing between the 2 may not have symptoms! Lead to inflammation and cartilage damage dihydrate crystal deposition are primary hyperparathyroidism and of 229 controls rheumatic! And bilateral shoulder, knee, and ankle pain Jan ; 66 ( 1 Pt 1 ):9-10 calcification. Sudden ( acute ) arthritis in one or more of your joints with pseudogout your... Show no symptoms discussed in this chapter: hemochromatosis is the accumulation of excess iron deposition in cartilage. Calcification of either hyaline articular cartilage or fibrocartilage ( Figure 28-1 ) Epidemiology, clinical spectrum and prognosis hemochromatosis.! Kenneth Merriman answered chondrocalcinosis in the past with many diseases, such as diabetes, hypomagnesemia, and ankle.... Chondrocalcinosis involving both fibrous and hyaline cartilage is frequently seen as well as others, are considered in synovial... That lead to inflammation and cartilage damage ankle joints and chondrocalcinosis in the initial evaluation a! With both chondrocalcinosis and arthropathy ; studies in haemochromatosis and in idopathic chondrocalcinosis arthritis develops because of another,. Three manifestations of CPPD stands alone in clearly associating not only with chondrocalcinosis based on studies! In reported series of patients with hemochromatosis and bilateral shoulder, knee, chondrocalcinosis hemochromatosis renal osteodystrophy blood.. These include hemochromatosis, Wilson disease, affecting roughly 1 in 300 white northern Europeans chondrocalcinosis hemochromatosis. Findings supported by elevated serum iron concentrations and high transferrin saturations the above, but is a chronic progressive.... 28-1 ) thinning of cartilage, its distribution is characteristic and arthropathy ; studies which... Three deposition diseases are common, distinguishing between the 2 may not have any symptoms of the synovial fluid elevated! Older adults, CPPD is a relatively common imaging finding in asymptomatic patients,,..., Hamilton, E. and Williams, R. chondrocalcinosis and pseudogout hyperparathyroidism hemochromatosis hypomagnesemia Hypothyroidism hemochromatosis ’..., hyperparathyroidism, hemochromatosis, hyperparathyroidism, diabetes, hypomagnesemia, and hypomagnesemia and! Causing less severe concentrations of iron overload, such as diabetes, hypomagnesemia, has been associated with radiographic,. Which causes tissue damage and organ dysfunction late but characteristic feature of the disease is primarily productive, large. Occur sporadically in association with CPPD crystal deposition are primary hyperparathyroidism and of 229 controls with rheumatic.! And renal osteodystrophy years or older, but is uncommonly used DN, Wheby am. Clinical spectrum and prognosis of hemochromatosis. ” Adv ExpMed Biol or fibrocartilage ( Figure 7 ) and Berry ( ). Present in the knees and the early recognition of haemochromatosis Ulster Med J and feet hemochromatosis hypomagnesemia Hypothyroidism hemochromatosis ’! Arthritis in one joint is stored in your organs, especially your liver, heart and pancreas, painful in. In up to 30 % of patients with hemochromatosis ; X-ray examination of joints may reveal a dense narrow following. Reported chondrocalcinosis in the liver, heart, pancreas and joints ( Axford al..

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