Prenatal diagnosis of Bardet Biedl Syndrome: A case report

Keyphrases

• Antepartum Surveillance 20%
• Asian Ethnicity 20%
• Ataxia 20%
• Autosomal Recessive 20%
• Baby Born 20%
• Bardet-Biedl Syndrome 100%
• Bengali 20%
• Clinical Management 20%
• Clinical Suspicion 20%
• Cone-rod Dystrophy 20%
• Consanguinity 20%
• Developmental Delay 20%
• Early Adulthood 20%
• Family History 20%
• Fetal Magnetic Resonance Imaging 20%
• Genetic Defects 20%
• Genetic Diagnosis 20%
• Hypogonadism 20%
• Late childhood 20%
• Laurence-Moon-Bardet-Biedl Syndrome 20%
• Learning Disabilities 20%
• Magnetic Resonance Findings 20%
• Major Features 20%
• Multigene Sequencing 20%
• Nystagmus 20%
• Obesity 20%
• Polydactyly 20%
• Prenatal Diagnosis 100%
• Primary Cilia 20%
• Renal Anomalies 20%
• Sequencing Technology 20%
• Speech Disorders 20%
• Syndrome-based 20%

Medicine and Dentistry

• Ataxia 16%
• Autosomal Recessive Inheritance 16%
• Bardet-Biedl Syndrome 100%
• Clinical Management 16%
• Cone Rod Dystrophy 16%
• Consanguinity 16%
• Developmental Delay 16%
• Family History 16%
• Genetic Disorder 16%
• Hypogonadism 16%
• Kidney Malformation 16%
• Learning Disability 16%
• Magnetic Resonance Imaging 16%
• Polydactyly 16%
• Prenatal Diagnosis 100%
• Primary Cilium 16%
• Speech Disorder 16%
• Symptomatic Treatment 16%