Congenital cutis laxa and lysyl oxidase deficiency

doi:10.1111/j.1399-0004.1997.tb02430.x

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Article

Congenital cutis laxa and lysyl oxidase deficiency

1 Feb 1997

Abstract excerpt

We report two phenotypically similar patients with primary cutis laxa associated with deficiency of lysyl oxidase, an extracellular copper enzyme the gene for which is located on chromosome 5. Previous reports of this condition have had characteristic occipital projections, abnormality of copper metabolism and X-linked inheritance. The two reported patients have no occipital projections, normal copper metabolism,...

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PMID: 9111998
DOI: 10.1111/j.1399-0004.1997.tb02430.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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