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Sebastian syndrome

Also Known As:
Sebastian platelet syndrome
Networked: 18 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Kunishima, Shinji: 4 articles (04/2014 - 01/2003)
2. Greinacher, Andreas: 2 articles (09/2007 - 03/2002)
3. Nichols, William L: 2 articles (11/2003 - 03/2002)
4. White, James G: 2 articles (11/2003 - 03/2002)
5. Kuzmanović, Milos: 1 article (04/2014)
6. Putnik, Jovana: 1 article (04/2014)
7. Paripović, Aleksandra: 1 article (04/2014)
8. Bogdanović, Radovan: 1 article (04/2014)
9. Stajić, Natasa: 1 article (04/2014)
10. Katsura, Ken-ichiro: 1 article (08/2008)

Related Diseases

1. Thrombocytopenia (Thrombopenia)
2. Hereditary Nephritis (Alport Syndrome)
3. Deafness (Deaf Mutism)
04/01/2009 - "Patients initially diagnosed with MHA and/or Sebastian syndrome can subsequently develop nephritis, deafness, and/or cataracts. "
11/15/2000 - "Other features of Alport syndrome, though, including deafness, cataracts, and nephritis, are absent in Sebastian platelet syndrome. "
04/01/2014 - "The group of autosomal dominant disorders - Epstein syndrome, Sebastian syndrome, Fechthner syndrome and May-Hegglin anomaly - are characterised by thrombocytopenia with giant platelets, inclusion bodies in granulocytes and variable levels of deafness, disturbances of vision and renal function impairment. "
04/01/1995 - "Sebastian platelet syndrome is an hereditary thrombocytopenia with giant platelets and inclusion bodies in the granulocytes consisting of dispersed filaments, clusters of ribosomes and a few segments of rough and smooth endoplasmic reticulum at the ultrastructural level, similar to those observed in Fechtner syndrome (a variant of the Alport syndrome)--Sebastian platelet syndrome lacks the additional clinical features such as high frequency deafness, congenital cataract, and chronic interstitial nephritis. "
07/15/2003 - "May-Hegglin anomaly (MHA), Fechtner syndrome (FTNS), Sebastian syndrome (SBS), and Epstein syndrome (EPS) are a group of rare, autosomal dominant disorders characterized by thrombocytopenia, giant platelets, and Döhle-like inclusion bodies, together with variable manifestations of Alport-like symptoms that include high-tone sensorineural deafness, cataracts, and nephritis. "
4. Cataract (Cataracts)
5. Nephritis

Related Drugs and Biologics

1. Fechtner syndrome
2. May-Hegglin anomaly
3. Epstein syndrome
4. Myosin Heavy Chains (Myosin Heavy Chain)