Andere Kunden interessierten sich auch für
![Le Syndrome Bardet-Biedl en Tunisie]( "Le Syndrome Bardet-Biedl en Tunisie")
Le Syndrome Bardet-Biedl en Tunisie43,99 €![Mutationsanalysen in BBS1 bei Patienten mit Bardet-Biedl-Syndrom]( "Mutationsanalysen in BBS1 bei Patienten mit Bardet-Biedl-Syndrom")
Mutationsanalysen in BBS1 bei Patienten mit Bardet-Biedl-Syndrom53,90 €![Engelmann syndrome]( "Engelmann syndrome")
Engelmann syndrome22,99 €![Costello syndrome]( "Costello syndrome")
Costello syndrome25,99 €![Rett Syndrome mutations: molecular alterations at neuronal synapses]( "Rett Syndrome mutations: molecular alterations at neuronal synapses")
Rett Syndrome mutations: molecular alterations at neuronal synapses32,99 €![Relation of some gene polymorphisms with metabolic syndrome in women]( "Relation of some gene polymorphisms with metabolic syndrome in women")
Relation of some gene polymorphisms with metabolic syndrome in women27,99 €![Down Syndrome in Oman]( "Down Syndrome in Oman")
Down Syndrome in Oman34,99 €
High Quality Content by WIKIPEDIA articles! The Bardet-3Biedl syndrome is a ciliopathic human genetic disorder that produces many effects and affects many body systems. It is characterized principally by obesity, retinitis pigmentosa, polydactyly, mental retardation, hypogonadism, and renal failure in some cases. "Bardet-Biedl syndrome is a pleiotropic disorder with variable expressivity and a wide range of clinical variability observed both within and between families. The main clinical features are rod-cone dystrophy, with childhood-onset visual loss preceded by night blindness; postaxial polydactyly; truncal obesity that manifests during infancy and remains problematic throughout adulthood; specific learning difficulties; male hypogenitalism and complex female genitourinary malformations; and renal dysfunction, a major cause of morbidity and mortality.