Gitelman syndrome disclosed by calcium pyrophosphate deposition disease: Early diagnosis by ultrasonographic study [PDF]
Gitelman's syndrome is a rare autosomal-recessive tubular disorder characterized by hypomagnesemia and hypocalciuria associated to hypokalemia. The clinical spectrum is wide and usually characterized by chronic fatigue, cramps, muscle weakness and ...
Zabotti, Alen +5 more
core +2 more sources
بررسی فراوانی کندروکلسينوز زانو در بيماران مبتلا به استئوآرتريت زانو مراجعه کننده به درمانگاههای روماتولوژی دانشگاه علوم پزشکی ايران(سال 80-1379) [PDF]
در اين مطالعه توصيفی با هدف تعيين فراوانی کندروکلسينوز زانو در مبتلايان به آرتروز زانو که به درمانگاههای روماتولوژی مراجعه کرده بودنـــد و سن بالای 40 سال داشتنـــد انجام شد. طی اين بررسی 65 بيمار مبتلا به آرتروز زانو با متوسط سنی 30/59 سال (1206/9=SD) و
احمدی, فریده +2 more
core
Advancing Clinical Medicine with Raman Spectroscopy: Current Trends and Future Perspectives
Raman spectroscopy and microscopy may become excellent tools in clinical medicine, including hematology, oncology, infectious diseases, neurology, gastroenterology, reproductive medicine, rheumatology, and cardiovascular research. However, many challenges such as signal interference, standardization issues, and limited clinical application need to be ...
Jiří Bufka +5 more
wiley +1 more source
ABSTRACT Chondrocalcinosis (CCAL), also known as calcium pyrophosphate dihydrate deposition disease (CPPDD), is a frequent multifactorial condition in the elderly, but there are two rare autosomal dominant Mendelian forms, CCAL1 (OMIM %600668) and CCAL2. Only three families with molecularly proven CCAL1 have been reported.
Anna‐Christina Pansa +4 more
wiley +1 more source
Efficacy of Anakinra for Various Types of Crystal-Induced Arthritis in Complex Hospitalized Patients: A Case Series and Review of the Literature [PDF]
International audienceBackground. There are few data on anakinra use after failure of conventional medications for crystal-induced peripheral arthritis and/or crowned dens syndrome among complex hospitalized patients. Methods. We retrospectively analyzed
Aouba, Achille +9 more
core +7 more sources
Recurrent Nephrolithiasis and Beyond: The Long Diagnostic Odyssey of a Case of CLDN16 Mutation
ABSTRACT Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis (FHHNC) is a rare tubulopathy resulting from mutations in the CLDN16 and CLDN19 genes. The affected individuals commonly present with polyuria, polydipsia, excessive urinary magnesium (Mg) and calcium (Ca) wasting, nephrocalcinosis, nephrolithiasis, recurrent urinary tract ...
Abdullah Al Noman Bhuiyan +4 more
wiley +1 more source
Diffuse articular chondrocalcinosis [PDF]
Chondrocalcinosis is a disease caused by joint deposition of calciumphyrophosphate dehydrate crystals, which can lead to many differentclinical presentations.
Ana Luisa Vanalle Ferrari +1 more
doaj
Pseudogout Diagnosed By Point-of-care Ultrasound [PDF]
A 71-year-old male presented to the emergency department (ED) for worsening right knee pain for the prior 3-4 weeks. Point-of-care ultrasound (POCUS) of the right knee showed a pseudo-double contour sign.
Bulbin, David H. +3 more
core
First Report of Intervertebral Disc Calcification in a Black Child in Sub‐Saharan Africa
Standard X‐ray of the cervical spine from the front and in profile. Blurred appearance of the C2–C3 and C3–C4 vertebral endplates and calcification (orange arrow) in the intervertebral disc of C2–C3. ABSTRACT We report an intervertebral disc calcification in a Black African child who had consulted us for neck pain. The diagnosis of C2–C3 intervertebral
Yamyelle Enselme Zongo +7 more
wiley +1 more source
An unusual location of gouty panniculitis: A case report. [PDF]
Gouty panniculitis, characterised by the deposition of monosodium urate crystals in subcutaneous tissue, is a rare clinical manifestation of gout. The case of a 67-year-old man is reported, who presented an erythematous nodule on the upper part of the ...
Brunel, C. +5 more
core +1 more source

