里什纳-汉哈特综合征（眼皮肤酪氨酸血症，Ⅱ型酪氨酸血症）。 - Suppr

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超能文献

Richner-Hanhart syndrome (oculocutaneous tyrosinaemia, tyrosinaemia type II).

作者信息

Paige D G, Clayton P, Bowron A, Harper J I

机构信息

Department of Dermatology, Hospitals for Sick Children, London.

出版信息

J R Soc Med. 1992 Dec;85(12):759-60. doi: 10.1177/014107689208501216.

DOI:10.1177/014107689208501216

PMID:1362969

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1293768/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4976/1293768/3f7486cf7f0e/jrsocmed00104-0061-a.jpg

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Richner-Hanhart syndrome (oculocutaneous tyrosinaemia, tyrosinaemia type II).里什纳-汉哈特综合征（眼皮肤酪氨酸血症，Ⅱ型酪氨酸血症）。

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本文引用的文献

Richner-Hanhart syndrome (tyrosinaemia-II) (report of four cases without ocular involvement).

Br J Dermatol. 1981 Apr;104(4):469-75. doi: 10.1111/j.1365-2133.1981.tb15320.x.

Dietary management of oculocutaneous tyrosinemia in an 11-year-old child.一名11岁儿童眼皮肤型酪氨酸血症的饮食管理

Am J Dis Child. 1983 Oct;137(10):995-1000. doi: 10.1001/archpedi.1983.02140360055018.

Successful dietary control of tyrosinemia II.

J Am Acad Dermatol. 1983 Oct;9(4):533-9. doi: 10.1016/s0190-9622(83)70165-9.

Tyrosinemia with plantar and palmar keratosis and keratitis.

J Pediatr. 1973 Nov;83(5):798-805. doi: 10.1016/s0022-3476(73)80372-5.

Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II.

Hum Genet. 1987 Dec;77(4):352-8. doi: 10.1007/BF00291426.

Outcome in tyrosinaemia type II.II型酪氨酸血症的结局

Arch Dis Child. 1991 Oct;66(10):1249-50. doi: 10.1136/adc.66.10.1249.

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