Literature DB >> 3380397

Aspects of treatment of homocystinuria: an illustrative case report.

D H Pullon1.   

Abstract

Cystathionine beta synthase deficiency homocystinuria is a heritable disorder most common in those of Irish descent. Therapy may prevent intellectual deficiency and dislocation of the ocular lenses. A female with this condition treated from the neonatal period to late adolescence is reported, including the use of betaine and antithrombotic drugs in management.

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Year:  1988        PMID: 3380397

Source DB:  PubMed          Journal:  N Z Med J        ISSN: 0028-8446


  2 in total

1.  Delayed diagnosis of homocystinuria in a myopic.

Authors:  C Capoferri; C Besana
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

Review 2.  Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.

Authors:  Andrew A M Morris; Viktor Kožich; Saikat Santra; Generoso Andria; Tawfeg I M Ben-Omran; Anupam B Chakrapani; Ellen Crushell; Mick J Henderson; Michel Hochuli; Martina Huemer; Miriam C H Janssen; Francois Maillot; Philip D Mayne; Jenny McNulty; Tara M Morrison; Helene Ogier; Siobhan O'Sullivan; Markéta Pavlíková; Isabel Tavares de Almeida; Allyson Terry; Sufin Yap; Henk J Blom; Kimberly A Chapman
Journal:  J Inherit Metab Dis       Date:  2016-10-24       Impact factor: 4.982

  2 in total

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