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Electroretinography and diagnosis of the Laurence-Moon-Bardet-Biedl syndrome in childhood.

Bardet-Biedl Syndrome with end stage renal disease

I stopped eating all the wrong stuff and started exercising to lose extra weight." Anneba, of Erdington, Birminghan, suffered from Laurence-Moon-Bardet-Biedl syndrome.

'I conquered my non-stop eating hell'

It wasn't until four years later that his parents would discover Daniel was suffering from a rare genetic condition called Laurence-Moon-Bardet-Biedl Syndrome (LMBBS), which would leave him overweight and nearly blind.

I was born with two extra fingers but rare genetic disorder was undetected for years; The Sunday Mercury is backing a PS1 million campaign to set up Europe's first Rare Disease Centre in Birmingham. ANUJI VARMA meets one of the patients who will benefit

INTRODUCTION: Laurence-Moon-Bardet-Biedl syndrome (LMBBS) is a rare, genetically heterogeneous, autosomal recessive disorder characterized by early onset retinitis pigmentosa, post axial polydactyly, central obesity, mental retardation, hypogonadism and kidney structural abnormalities or functional impairment.

CASE REPORT: Here is a joint family of 11 members, which had 7 affected members with various sub syndromes of Laurence-Moon-Bardet-Biedl Syndrome; all the affected members had supernumerary teeth which was a rare feature in this variant of Laurence-Moon-Bardet-Biedl Syndrome.

A variant of Laurence-moon-bardet-biedl syndrome supernumerary teeth

Among these, 4 children (2.4%) had unknown syndrome, 5(3%) had Turner's syndrome, 2 children (1.2%) Laurence-Moon-Bardet-Biedl syndrome and 2(1.2%) Noonan syndrome.

Causes of short stature identified in children presenting at a tertiary care hospital in Multan Pakistan

Laurence-Moon-Bardet-Biedl Syndrome Network 18 Strawberry Hill Windsor, CT 06095 (203) 688-7880 1,4

National resources for specific disabilities and conditions

Laurence-Moon-Bardet-Biedl syndrome

Laurence-Biedl syndrome