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The Richner-Hanhart syndrome: report of a case with associated tyrosinemia.

作者信息

Bienfang D C, Kuwabara T, Pueschel S M

出版信息

Arch Ophthalmol. 1976 Jul;94(7):1133-7. doi: 10.1001/archopht.1976.03910040045009.

DOI:10.1001/archopht.1976.03910040045009
PMID:180943
Abstract

The Richner-Hanhart syndrome with tyrosinemia was recognized in a mentally retarded adolescent boy. The clinical manifestations, including hyperkeratosis of the volar aspects of the hands and feet, thickening of the conjunctival epithelium, and corneal opacities, as well as biochemical aberrations of tyrosine metabolism, responded to specific treatment with a diet low in phenylalanine and tyrosine. Light and electron microscopical studies illustrate the underlying conjunctival pathologic changes.

摘要

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Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations.I 型酪氨酸血症的诊断和治疗:美国和加拿大共识小组的回顾和建议。
Genet Med. 2017 Dec;19(12). doi: 10.1038/gim.2017.101. Epub 2017 Aug 3.
2
Metabolic syndromes with dermatologic manifestations.伴有皮肤表现的代谢综合征
Clin Rev Allergy. 1986 Feb;4(1):101-24. doi: 10.1007/BF02991190.
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The eye and inherited metabolic disease: a review.眼睛与遗传性代谢疾病:综述
J R Soc Med. 1988 May;81(5):286-90. doi: 10.1177/014107688808100517.