hepatosplenomegaly sentence in Hindi
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- The hallmark clinical and laboratory features include high fever, hepatosplenomegaly, lymphadenopathy, pancytopenia, liver dysfunction, disseminated intravascular coagulation, hypofibrinogenemia, hyperferritinemia, and hypertriglyceridemia.
- The toxicity associated with galactose-1-phosphate uridylyltransferase deficiency is associated with symptoms of hepatosplenomegaly and mental retardation in addition to the cataracts caused by galactitol buildup.
- This is a rare ( less than 100 reported cases ) autosomal recessive disorder characterized by partial albinism, hepatosplenomegaly, pancytopenia, hepatitis, immunologic abnormalities, and lymphohistiocytosis.
- Vaquez described the disease in a 40-year-old male suffering from chronic cyanosis, distended veins, vertigo, dyspnea, hepatosplenomegaly, palpitations and marked erythrocytosis.
- Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises.
- Because glycosylation is known to be critical for numerous immune-related proteins, these patients likely present with additional abnormalities including neutropenia, hemolytic anemia, hepatosplenomegaly, and neutropenia.
- Hepatosplenomegaly can occur as the result of acute viral hepatitis, infectious mononucleosis, and histoplasmosis or it can be the sign of a serious and life-threatening lysosomal storage disease.
- Babies exposed, in utero, can have deformities, delays in development, or seizures along with many other problems such as rash, fever, hepatosplenomegaly, anemia, and jaundice.
- They may have unusual facial features that are often described as " coarse, " seizures, bone malformations, enlarged liver and spleen ( hepatosplenomegaly ), and an enlarged heart ( cardiomegaly ).
- Symptoms may begin early in life or in adulthood and mainly affect the liver, spleen, and bone . enlarged spleen ( together hepatosplenomegaly ) are common; the spleen can rupture and cause additional complications.
- Initial symptoms include fever, chills, headaches, pain behind the eyes, light sensitivity, muscle pain, generalized malaise, abdominal pain, hepatosplenomegaly, nausea and vomiting, and a flat or pimply rash.
- Classified as an inborn error of metabolism, mevalonate kinase deficiency usually results in developmental delay, hypotonia, anemia, hepatosplenomegaly, various dysmorphic features, mental retardation, an overall failure to thrive and several other features.
- Some forms of primary hypertriglyceridemia can lead to specific symptoms : both familial chylomicronemia and primary mixed hyperlipidemia include skin symptoms ( eruptive xanthoma ), eye abnormalities ( lipemia retinalis ), hepatosplenomegaly ( enlargement of the liver and spleen ), and neurological symptoms.
- Mother exposure to cytomegalovirus can cause microcephaly, cerebral calcifications, blindess, chorioretinitis ( which can cause blindness ), hepatosplenomegaly, and meningoencephalitis in fetuses . cerebral calcifications means certain areas of the brain have atypical calcium deposits, and meningoencephalitis is the enlargement of the brain.
- Individuals who are homozygous for a specific mutation ( K404E ) or compound heterozygous with a null allele in " CPOX " have a more severe erythropoietic porphyria, harderoporphyria, characterized by neonatal jaundice, hyperbilirubinemia, hepatosplenomegaly and skin lesions upon exposure to ultraviolet light.
- Symptoms include life-threatening illnesses such as jaundice, hepatosplenomegaly ( enlarged spleen and liver ), hypoglycemia, renal tubular dysfunction, muscle hypotonia ( decreased tone and muscle strength ), sepsis ( presence of harmful bacteria and their toxins in tissues ), and cataract among others.
- Waldenstr�m first described, in 1944, patients suffering from a disease that has subsequently been named for him, Waldenstrom's macroglobulinema, a " hyperviscosity syndrome " in which symptoms are caused by abnormal lymphocytes which prevent normal bone marrow function, causing anemia and hepatosplenomegaly, and which secrete large immunoglobulins, causing bleeding difficulties.
- Even more recently, a study was done in 2013 on a family that showed history of autosomal recessive inheritance of HGF . The study did not dismiss the return of HGF after treatment but did claim that general surgical intervention after scaling and root planning of teeth supplemented with good oral hygiene is good enough to prevent the re-occurrence of HGF . This case study also acknowledged how HGF can be part of a multi-system syndrome associated with disorders such as Zimmermann Laband syndrome ( ear, nose, bone, and nail defects with hepatosplenomegaly ), Rutherford syndrome, microphthalmia, mental retardation, athetosis, and hypopigmentation ), Murray-Puretic Drescher syndrome, and Ramon syndrome.
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hepatosplenomegaly sentences in Hindi. What are the example sentences for hepatosplenomegaly? hepatosplenomegaly English meaning, translation, pronunciation, synonyms and example sentences are provided by Hindlish.com.