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- Kearns–Sayre_syndrome abstract "Kearns–Sayre syndrome (abbreviated KSS) also known as oculocraniosomatic disease or Oculocraniosomatic neuromuscular disease with ragged red fibers is a mitochondrial myopathy with a typical onset before 20 years of age. KSS is a more severe syndromic variant of chronic progressive external ophthalmoplegia (abbreviated CPEO), a syndrome that is characterized by isolated involvement of the muscles controlling eyelid movement (levator palpebrae, orbicularis oculi), and those controlling eye movement (extra-ocular muscles). This results in ptosis and ophthalmoplegia respectively. KSS involves a triad of the already described CPEO, as well as bilateral pigmentary retinopathy, and cardiac conduction abnormalities. Other areas of involvement can include cerebellar ataxia, proximal muscle weakness, deafness, diabetes mellitus, growth hormone deficiency, hypoparathyroidism, or other endocrinopathies. In both of these diseases, muscle involvement may begin unilateral but always develops into a bilateral deficit, and the course is progressive. This discussion is limited specifically to the more severe and systemically involved variant; KSS".
- Kearns–Sayre_syndrome wikiPageID "3021700".
- Kearns–Sayre_syndrome wikiPageRevisionID "591989001".
- Kearns–Sayre_syndrome diseasesdb "7137".
- Kearns–Sayre_syndrome emedicinesubj "article".
- Kearns–Sayre_syndrome emedicinetopic "950897".
- Kearns–Sayre_syndrome genereviewsname "Mitochondrial DNA Deletion Syndromes".
- Kearns–Sayre_syndrome genereviewsnbk "NBK1203".
- Kearns–Sayre_syndrome icd "277.87".
- Kearns–Sayre_syndrome icd "H49.8".
- Kearns–Sayre_syndrome meshid "D007625".
- Kearns–Sayre_syndrome name "Kearns-Sayre syndrome".
- Kearns–Sayre_syndrome omim "530000".
- Kearns–Sayre_syndrome subject Category:Disorders_of_ocular_muscles,_binocular_movement,_accommodation_and_refraction.
- Kearns–Sayre_syndrome subject Category:Mitochondrial_diseases.
- Kearns–Sayre_syndrome subject Category:Rare_diseases.
- Kearns–Sayre_syndrome subject Category:Syndromes.
- Kearns–Sayre_syndrome type Disease.
- Kearns–Sayre_syndrome type Situation.
- Kearns–Sayre_syndrome comment "Kearns–Sayre syndrome (abbreviated KSS) also known as oculocraniosomatic disease or Oculocraniosomatic neuromuscular disease with ragged red fibers is a mitochondrial myopathy with a typical onset before 20 years of age.".
- Kearns–Sayre_syndrome label "Kearns–Sayre syndrome".
- Kearns–Sayre_syndrome label "Syndrome de Kearns-Sayre".
- Kearns–Sayre_syndrome label "Syndroom van Kearns-Sayre".
- Kearns–Sayre_syndrome label "Síndrome de Kearns-Sayre".
- Kearns–Sayre_syndrome label "Zespół Kearnsa-Sayre'a".
- Kearns–Sayre_syndrome sameAs Kearns%E2%80%93Sayre_syndrome.
- Kearns–Sayre_syndrome sameAs Síndrome_de_Kearns-Sayre.
- Kearns–Sayre_syndrome sameAs Syndrome_de_Kearns-Sayre.
- Kearns–Sayre_syndrome sameAs Syndroom_van_Kearns-Sayre.
- Kearns–Sayre_syndrome sameAs Zespół_Kearnsa-Sayre'a.
- Kearns–Sayre_syndrome sameAs Q2605012.
- Kearns–Sayre_syndrome sameAs Q2605012.
- Kearns–Sayre_syndrome wasDerivedFrom Kearns–Sayre_syndrome?oldid=591989001.