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1,172 Possible Causes for Steroid, Sulfatase

  • X-Linked Ichthyosis

    Deficiency of steroid sulfatase was found in the male patient, while in his mother enzyme levels were in the heterozygous range.[ncbi.nlm.nih.gov] The decreased enzyme activity is due to the absence of the expression of enzyme (steroid sulfatase) protein.[ncbi.nlm.nih.gov] We have isolated several cDNA clones from a lambda gt11 expression library by screening with antibodies prepared against the microsomal enzyme steroid sulfatase, which is[ncbi.nlm.nih.gov]

  • Recessive X-Linked Ichthyosis

    Normal human epidermis, the tissue most affected clinically, also expresses steroid sulfatase activity.[ncbi.nlm.nih.gov] […] or to react with normal steroid sulfatase on immunoblot.[ncbi.nlm.nih.gov] Abstract Steroid sulphatase (STS) activity was measured with tritiated dehydroepiandrosterone sulphate (DHEAS) and oestrone sulphate (OES) in leucocytes as well as in skin[ncbi.nlm.nih.gov]

  • Ichthyosis and Male Hypogonadism

    Keywords Public Health Steroid Hypogonadism Steroid Sulphatase Steroid Sulphatase Deficiency These keywords were added by machine and not by the authors.[springerlink.com] STS deficiency also occurs as a manifestation of multiple sulfatase deficiency, an extremely rare autosomal recessive disorder affecting the activity of many sulfatases and[ommbid.mhmedical.com] Placental sulfatase deficiency: maternal and fetal expression of steroid sulfatase defi- ciency and X-linked ichthyosis.[passeidireto.com]

  • Autosomal Recessive Steroid-Resistant Nephrotic Syndrome

    Of these, seven (11.2%) were initially found to be steroid resistant, while the others were steroid responsive.[cags.org.ae] * Mucopolysaccharidosis (MPS) type IIIA (Sanfilippo A) Mucopolysaccharidosis (MPS) type IIIB (Sanfilippo B) Mucopolysaccharidosis (MPS) type IIIC (Sanfilippo C) Multiple sulfatase[jscreen.org] . / NPHS2 mutations in steroid-resistant nephrotic syndrome : a mutation update and the associated phenotypic spectrum .[research-information.bristol.ac.uk]

  • Mucopolysaccharidosis 4

    AEs that resulted in infusion interruptions and/or discontinuations could be managed with symptomatic treatment (oxygen, IV steroids, IV antihistamines, or IV fluids) and[nature.com] Turnaround Time 2 weeks CPT Code(s) 82657 Cost 200.00 Enzymes N-acetyl-galactosamine-6-sulfatase Beta-galactosidase Morquio syndrome is characterized by short stature and[ggc.org] 8001980 Morquio A syndrome: cloning, sequence, and structure of the human N-acetylgalactosamine 6-sulfatase (GALNS) gene Morris, CP , Guo, XH , Apostolou, S , Hopwood, JJ[reactome.org]

  • Mucopolysaccharidosis 2

    Such reactions are generally managed by slowing the infusion rate and administering anti-histamines and/or steroids [ 71 ].[rheumatology.oxfordjournals.org] Mucopolysaccharidosis type II (MPS II; also known as Hunter syndrome) is an X-linked multisystem disorder resulting from the defective activity of the enzyme iduronate-2-sulfatase[ncbi.nlm.nih.gov] Patients with hip dysplasia may be given non-steroidal anti-inflammatory medications. CARPAL TUNNEL SYNDROME Carpal tunnel syndrome is a common problem in MPS.[encyclopedia.com]

  • Tolosa-Hunt Syndrome

    Abstract Some but not all patients with Tolosa-Hunt syndrome (THS) have dramatic responses to steroid treatment.[ncbi.nlm.nih.gov] Aril sulfatase B. Pitanoil-koenzim A hidroksilase C. Beta-gukosilase D. Alfa-galaktosidase E.[brainscape.com] SPIR MRI may be useful not only to support a diagnosis of Tolosa-Hunt syndrome, but also to follow-up the disease course and to manage steroid treatment.[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis

    J Steroid Biochem Mol Biol. 2007, 105: 37-45.[dx.doi.org] Mucopolysaccharidosis type II (MPS II; also known as Hunter syndrome) is an X-linked multisystem disorder resulting from the defective activity of the enzyme iduronate-2-sulfatase[ncbi.nlm.nih.gov] Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is X-linked recessive lysosomal storage disorder resulting from the defective activity of the enzyme iduronate-2-sulfatase[ncbi.nlm.nih.gov]

  • Granulomatous Mastitis

    In our case, topical steroid therapy was applied four days per week bid along with oral steroid treatment.[doi.org] […] deficiency GABEB Gabriele-de Vries syndrome Gaisböck syndrome Galactocerebrosidase deficiency Galactokinase deficiency Galactokinase deficiency galactosemia Galactosamine-6-sulfatase[orpha.net] 10.7 %), and no side effects or steroid-related complications occurred.[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis 4A

    […] relieve and avoidance of complications due to lesions of the nervous system, heart and respiratory tract, which may be achieved by means of surgery, administration of non-steroidal[symptoma.com] Homepage Rare diseases Search Search for a rare disease Mucopolysaccharidosis type 4A ORPHA:309297 Synonym(s): GALNS deficiency Galactosamine-6-sulfatase deficiency MPS4A[orpha.net] Steroid induced osteopenia should be addressed while positioning the patient. Maintenance steroid therapy intraoperatively prevents adrenal crisis.[joacp.org]

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