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Case Reports
. 2014 Oct-Dec;26(4):625-7.

Laurence Moon Bardet Biedl Syndrome with anaemia

  • PMID: 25672202
Case Reports

Laurence Moon Bardet Biedl Syndrome with anaemia

Mariam Asif et al. J Ayub Med Coll Abbottabad. 2014 Oct-Dec.

Abstract

Laurence Moon Bardet Biedl Syndrome is a rare genetic disorder. Consanguineous marriage is usually the common cause. Principal features of Bardet Biedl Syndrome are red cone dystrophy, obesity, polydactyl, hypogonadism and renal anomalies. The diagnosis was overlooked in our patient until he came in our hospital. We here report an infrequent case of autosomal recessive disorder with Anaemia.

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