Penetrating Keratoplasty for Corneal Amyloidosis in Familial Amyloidosis, Finnish Type

Mattila Jaakko S.; Krootila Kari; Kivelae Tero; Holopainen Juha M.

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Penetrating Keratoplasty for Corneal Amyloidosis in Familial Amyloidosis, Finnish Type

机译：芬兰型家族性淀粉样变性的穿透性角膜移植术治疗角膜淀粉样变性

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摘要

Purpose: To analyze the outcome of penetrating keratoplasty (PK) to the first eye for corneal amyloidosis in familial amyloidosis, Finnish type (FAF).

机译：目的：分析芬兰型（FAF）家族性淀粉样变性病对第一只眼的穿透性角膜移植手术（PK）的结果。

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《Ophthalmology 》 |2015年第3期| 共7页
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Mattila Jaakko S.; Krootila Kari; Kivelae Tero; Holopainen Juha M.;
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正文语种 eng
中图分类眼科学 ;
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1. Penetrating Keratoplasty for Corneal Amyloidosis in Familial Amyloidosis, Finnish Type [J] . Mattila Jaakko S., Krootila Kari, Kivelae Tero, Ophthalmology . 2015 ,第3期

机译：芬兰型家族性淀粉样变性的穿透性角膜移植术治疗角膜淀粉样变性
2. Danish type gelsolin related amyloidosis: 654G-T mutation is assoicated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type) [J] . Carl Peter J Maury, Mikko Lijestrom, Gudrun Boysen Journal of Clinical Pathology . 2000 ,第2期

机译：丹麦凝溶胶蛋白相关的淀粉样变性病：654G-T突变与在疾病上和临床上与654G-A突变引起的疾病（芬兰型家族性淀粉样变性）相关
3. Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family. [J] . Stewart HS, Parveen R, Ridgway AE, British journal of ophthalmology . 2000 ,第4期

机译：在一个英国家庭中，晚期发作性角膜营养不良伴系统性家族性淀粉样变性病，即淀粉样变性病V。
4. ATTR (THR59LYS) AMYLOIDOSIS WITH INVOLVEMENT OF HEART, PERIPHERAL AND AUTONOMIC NERVOUS SYSTEM, GUT AND SALIVARY GLANDS IN AN EGYPTIAN MAN, PREVIOUSLY DIAGNOSED AS "FAMILIAL AMYLOID NEUROPATHY OF PORTUGUESE TYPE" [C] . G.E Feurle, J.J. Liepnieks, M.D Benson, International Symposium on Amyloidosis . 2008

机译：attr（thr59lys）淀粉样蛋白症，在埃及人中的心脏，外周和自主神经系统，肠道和唾液腺腺体，以前被诊断为“葡萄牙语类型的家族淀粉样蛋白神经病变”
5. Studies of an Unusual Transthyretin Protein (Ttr Glu51_Ser52dup) Associated with Familial Amyloidosis. [D] . Abdullahi, Hassan A. 2017

机译：与家族性淀粉样变性病相关的异常甲状腺素蛋白（Ttr Glu51_Ser52dup）的研究。
6. Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type) [O] . C. P. Maury, M. Liljestrom, G. Boysen, 2000

机译：丹麦凝溶胶蛋白相关淀粉样变性病：654G-T突变与在疾病上和临床上与654G-A突变引起的疾病（芬兰型家族性淀粉样变性）相关
7. Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type) [O] . Maury, C. P., Liljestrom, M., Boysen, G., 2000

机译：丹麦凝溶胶蛋白相关淀粉样变性病：654G-T突变与在疾病上和临床上与654G-A突变引起的疾病（芬兰型家族性淀粉样变性）相关

Penetrating Keratoplasty for Corneal Amyloidosis in Familial Amyloidosis, Finnish Type

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