A rare case of the lenz syndrome

T. Sohil, K. Ketki, M. S. Rukmini, K. Nutan, M. Poornima

Research output: Contribution to journalArticle

Abstract

We are reporting here, a case of the Lenz syndrome in a neonate who was brought to the Paediatric OPD, Kasturba Medical Col-lege Hospital, Attavar, Mangalore India, with the complaints of poor suckling since birth and abnormal facial features. Altogether, the characteristic congenital abnormal findings in Lenz syndrome, which comprise of microophthalmia, ear anomalies, microcephaly, skeletal and digital deformities, and urogenital malformations were observed, with an exception of a dental anomaly. Dental abnor-malities were not pertinent, as the patient was a neonate.

Original languageEnglish
Pages (from-to)347-349
Number of pages3
JournalJournal of Clinical and Diagnostic Research
Volume7
Issue number2
DOIs
Publication statusPublished - 01-02-2013

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Pediatrics
Tooth
Newborn Infant
Microcephaly
Ear
India
Parturition
Syndromic 1 Microphthalmia

All Science Journal Classification (ASJC) codes

  • Clinical Biochemistry

Cite this

Sohil, T. ; Ketki, K. ; Rukmini, M. S. ; Nutan, K. ; Poornima, M. / A rare case of the lenz syndrome. In: Journal of Clinical and Diagnostic Research. 2013 ; Vol. 7, No. 2. pp. 347-349.
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A rare case of the lenz syndrome. / Sohil, T.; Ketki, K.; Rukmini, M. S.; Nutan, K.; Poornima, M.

In: Journal of Clinical and Diagnostic Research, Vol. 7, No. 2, 01.02.2013, p. 347-349.

Research output: Contribution to journalArticle

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