Literature DB >> 3438056

Ophthalmic midline dysgenesis in Kallmann syndrome.

M J Jaffe1, J Currie, J D Schwankhaus, R J Sherins.   

Abstract

Partial coloboma, observed only with transillumination techniques, occur in 16% of male patients diagnosed with Kallmann syndrome. This sign represents an additional midline defect in this multisystem disorder noted for midline dysgenesis. Its high incidence may be helpful in the diagnosis of this disorder although it does not appear to be the harbinger of any other ocular abnormality.

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Year:  1987        PMID: 3438056     DOI: 10.3109/13816818709031464

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  4 in total

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4.  A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review.

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  4 in total

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