Add to ORKGBardet-Biedl syndrome (BBS) is one of the rare autosomal recessive disorders that affect multiple organs of the body. The signs and symptoms of this condition vary among affected individuals, even among members of the same family. We present a case of BBS with features of hypogonadism and features such as marked central obesity, retinitis pigmentosa, polydactyly, renal abnormalities and mental retardation, along with a brief review of the literature. The patient had end stage renal disease and managed with dialysis. This case also exemplifies the need for multidisciplinary approach in the management of such cases
Bardet Biedl syndrome is a rare autosomal recessive condition with a wide spectrum of clinical featu...
Bardet-Biedl syndrome is rare. Although its diagnosis depends on cardinal clinical manifestations wh...
Background and Objectives Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive ciliopathy with ...
Bardet Biedl syndrome (BBS) is a rare autosomal recessive condition characterised by rod-cone dystro...
Abstract The Bardet-Biedl Syndrome is a rare autosomal recessive disorder with clinical and genetic ...
We studied four patients from two families manifesting impaired vision, obesity, hypogenitalism, pol...
Laurence-Moon-Bardet-Biedl syndrome is a rare congenital disorder, inherited in the autosomal recess...
Bardet-Biedl Syndrome (BBS) is a rarely seen autosomal recessive transfer disease characterised by r...
Bardet-Biedl syndrome (BBS) is an autosomal recessive condition with a wide spectrum of clinical fea...
Bardet Biedl syndrome is a rare autosomal recessive condition with a wide spectrum of clinical featu...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
PubMedID: 7793264Six patients with Bardet-Biedl syndrome who have been followed in our clinics for t...
Laurence Moon Bardet Biedl is a congenital syndrome which is rarely seen and accompanied by multipl ...
The Bardet–Biedl syndrome (BBS) is a rare ciliopathic autosomal-recessive disorder, with multiple or...
p.694-696Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disorder with clinical and geneti...
Bardet Biedl syndrome is a rare autosomal recessive condition with a wide spectrum of clinical featu...
Bardet-Biedl syndrome is rare. Although its diagnosis depends on cardinal clinical manifestations wh...
Background and Objectives Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive ciliopathy with ...
Bardet Biedl syndrome (BBS) is a rare autosomal recessive condition characterised by rod-cone dystro...
Abstract The Bardet-Biedl Syndrome is a rare autosomal recessive disorder with clinical and genetic ...
We studied four patients from two families manifesting impaired vision, obesity, hypogenitalism, pol...
Laurence-Moon-Bardet-Biedl syndrome is a rare congenital disorder, inherited in the autosomal recess...
Bardet-Biedl Syndrome (BBS) is a rarely seen autosomal recessive transfer disease characterised by r...
Bardet-Biedl syndrome (BBS) is an autosomal recessive condition with a wide spectrum of clinical fea...
Bardet Biedl syndrome is a rare autosomal recessive condition with a wide spectrum of clinical featu...
Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction...
PubMedID: 7793264Six patients with Bardet-Biedl syndrome who have been followed in our clinics for t...
Laurence Moon Bardet Biedl is a congenital syndrome which is rarely seen and accompanied by multipl ...
The Bardet–Biedl syndrome (BBS) is a rare ciliopathic autosomal-recessive disorder, with multiple or...
p.694-696Bardet-Biedl syndrome (BBS) is a rare autosomal recessive disorder with clinical and geneti...
Bardet Biedl syndrome is a rare autosomal recessive condition with a wide spectrum of clinical featu...
Bardet-Biedl syndrome is rare. Although its diagnosis depends on cardinal clinical manifestations wh...
Background and Objectives Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive ciliopathy with ...