メレトヤ症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/09/18 19:18:41」(JST)
[Wiki en表示]
Ardalan–Shoja–Kiuru syndrome is a clinical syndrome featuring hereditary gelsolin amyloidosis and retinitis pigmentosa.[1] This syndrome was first recognized by two Iranian physicians, Mohammad Ardalan and Mohammadali Shoja and Finnish neurologist Sari Kiuru-Enari in an Iranian family.[2] Hereditary gelsolin amyloidosis has originally been reported by Finnish ophthalmologist Jouko Meretoja and is known as Meretoja syndrome or Familial Amyloidosis, Finnish type.[3] In addition to the classic manifestations of Finnish type Familial Amyloidosis, cutis laxa, progressive peripheral neuropathy and corneal lattice dystrophy, some of the afflicted members of the Iranian family have retinitis pigmentosa.[1][2] This feature had not been previously reported with this type of amyloidosis. Ardalan–Shoja–Kiuru syndrome or hereditary gelsolin amyloidosis plus retintis pigmentosa has not been found outside this single Iranian family.[2]
References
- ^ a b Shokouhi G. and H. T. Khosroshahi. (2008) Ardalan–Shoja–Kiuru syndrome – hereditary gelsolin amyloidosis plus retinitis pigmentosa. Nephrol Dial Transplant 23(3):1071.
- ^ a b c Ardalan M. R., M. M. Shoja, and S. Kiuru-Enari. (2007) Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East. Nephrol Dial Transplant 22(1):272–5.
- ^ Kiuru S. (1998) Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide. Amyloid. 5(1):55–66.
UpToDate Contents
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English Journal
- Natural course of Finnish gelsolin amyloidosis.
- Nikoskinen T1, Schmidt EK1, Strbian D2, Kiuru-Enari S2, Atula S2.
- Annals of medicine.Ann Med.2015 Sep;47(6):506-11. doi: 10.3109/07853890.2015.1075063. Epub 2015 Sep 4.
- BACKGROUND: Finnish type of hereditary gelsolin amyloidosis (FGA) is one of the most common diseases of Finnish disease heritage. Existing FGA knowledge is based only on smaller patient series, so our aim was to elucidate the natural course of the disease in a comprehensive sample of patients and to
- PMID 26339870
- [Meretoja syndrome: Identification of a family and description of the corneal involvement by confocal microscopy].
- Bonnin N1, Borel A2, Daniel E3, Tiple A4, Joubert R3, Heng AE4, Chiambaretta F5.
- Journal français d'ophtalmologie.J Fr Ophtalmol.2015 Jun;38(6):e111-5. doi: 10.1016/j.jfo.2014.10.016. Epub 2015 Apr 23.
- PMID 25913657
- [The revised newest IC³D classification of corneal dystrophies].
- Seitz B1, Lisch W2, Weiss J3.
- Klinische Monatsblätter für Augenheilkunde.Klin Monbl Augenheilkd.2015 Mar;232(3):283-94. doi: 10.1055/s-0041-100774. Epub 2015 Mar 24.
- PURPOSE: This report suggests how corneal dystrophies (CDs) should be diagnosed at the slit lamp and specifies the new IC(3)D classification of CDs in 2015 which incorporates new information.METHODS: IC(3)D reviewed all peer-reviewed articles on CDs 2008 to 6/2014. Corneal dystrophy templates and an
- PMID 25803558
Japanese Journal
- Lattice corneal dystrophy associated with familial systemic amyloidosis (Meretoja's syndrome)
Related Links
- syndrome [sin´drōm] a combination of symptoms resulting from a single cause or so commonly occurring together as to constitute a distinct clinical picture. For specific syndromes, see under the name, such as adrenogenital ...
- Meretoja syndrome Meretoja's syndrome Meretoja, J Meretoja, J. Meretoja, J. Meretoja, J. meretricious meretricious meretriciously meretriciously meretriciousness meretriciousness Meretskov, Kirill Meretskov, Kirill Afanasevich ...
★リンクテーブル★
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- 英
- Meretoja syndrome
- 同
- アミロイドーシスV型 amyloidosis type V、フィンランド型アミロイドーシス Finland type amyloidosis
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