Our review is designed to help you maximize your score on the Neurodevelopmental Disabilities Exam. StatPearls questions and articles are linked directly to American Board of Psychiatry and Neurology® and American Osteopathic Board of Neurology and Psychiatry® content outlines. Each review course is designed to empower you to assess your knowledge and understanding of medical principles and concepts found on the Neurodevelopmental Disabilities Exam.
We have 249 Multiple-choice 1st, 2nd, and 3rd order questions with four detailed teaching points linked to 136 PubMed indexed review articles related to the Neurodevelopmental Disabilities Certification Examination. You can customize practice questions to anatomical and clinical Neurodevelopmental Disabilities Specialist subject areas. In addition, you will have access to a 250 question pre- and post-test Neurodevelopmental Disabilities Exam to help you target learning and identify areas that need further study. Analytics and reports allow you to compare your scores to other students.
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The StatPearls neurodevelopmental disabilities prep questions, neurodevelopmental disabilities review questions, and neurodevelopmental disabilities test questions will help you achieve a top score on the Neurodevelopmental Disabilities Certification Examination. 150 authors and 5 editors have contributed to the development of the Neurodevelopmental Disabilities Exam content, which is continuously refined and updated to improve your learning experience.
Neurodevelopmental Disabilities Exam Overview
How many hours is the Neurodevelopmental Disabilities Exam?
The Neurodevelopmental Disabilities Exam is 3 hours.
How many questions is the Neurodevelopmental Disabilities Exam?
The Neurodevelopmental Disabilities Exam is 150 questions.
What topics are covered on the Neurodevelopmental Disabilities Exam?
Topics include: Normal development: 4-6%, Neurogenetics: 8-12%, Cognitive disorders (intellectual disability, global developmental delay): 13-17%, Cognitive disorders (learning disabilities): 8-12%, Communication disorders, e.g., autism spectrum disorder, developmental speech and language disorders: 13-17%, Neurobehavioral disorders, e.g., ADHD, obsessive-compulsive disorder, oppositional defiant disorder, Tourette disorder: 8-12%, Motor disabilities, e.g., static and progressive encephalopathies, cerebral palsy, neuromuscular disorders, minor neuromotor dysfunction: 8-12%, Visual and auditory impairments: 4-6%, Neurodevelopmental disorders associated with major medical conditions, e.g., spina bifida, severely and profoundly disabled, low-birth-weight infants, multiple congenital anomalies: 6-8%, Rehabilitation, e.g., traumatic brain and spinal cord injuries, near-drowning: 4-6%, and Counseling, advocacy, and ethics, including research ethics: 6-8%
Neurodevelopmental Disabilities Exam MCQs (249)
Our question bank for the Neurodevelopmental Disabilities Exam covers four Cognitive Difficulty Levels:
- Cardiovascular - 6 questions
- Connective Tissue - 1 questions
- Ears Nose and Throat - 5 questions
- Endocrine and Metabolic - 23 questions
- Eyes - 12 questions
- Gastrointestinal - 4 questions
- Genetics - 115 questions
- Genitourinary - 1 questions
- Growth and Development - 142 questions
- Infectious - 1 questions
- Integument - 18 questions
- Musculoskeletal - 48 questions
- Nervous - 237 questions
- Nutrition - 3 questions
- Obstetric - 7 questions
- Oncologic - 6 questions
- Psychiatric Mental Health - 36 questions
- Pulmonary - 2 questions
- Renal - 3 questions
- Surgery - 3 questions
- Toxicology - 3 questions
- Teeth/Oral - 1 questions
- Manage Care and Comply Regulations - 1 questions
- Health Promotion & Maintenance (Prevent Problems) - 1 questions
- Basic Care and Comfort (Assist Daily Living Tasks) - 1 questions
- Pharm/Parenteral Therapy (Drugs/Vital Signs) - 4 questions
- Physiological Adaptation (Care Ill Patients) - 113 questions
- Psychosocial (Mental Health Patient/Family) - 20 questions
- Process (Analysis, Assess, Eval, Implement, Plan) - 138 questions
- Teaching/Learning (Promotes Behavior Change) - 2 questions
- Causes - 91 questions
- Classification - 36 questions
- Differential - 179 questions
- Epidemiology - 12 questions
- Evaluation Diagnostic Tests - 47 questions
- Evaluation Lab - 22 questions
- Evaluation Monitoring - 10 questions
- Evaluation Procedures - 22 questions
- Evaluation Radiologic - 95 questions
- Health Maint Prevention Public Health - 2 questions
- History Physical - 263 questions
- Legal - 1 questions
- Pathophysiology - 153 questions
- Patient Education - 6 questions
- Prognosis Complications - 139 questions
- Toxicology - 2 questions
- Treatment Medical - 32 questions
- Treatment Rehabilitation - 4 questions
- Treatment Surgical - 8 questions
- Healthcare Ethics - 1 questions
- Clinical Education - 3 questions
- Therapeutics (Drug treatment) - 3 questions
- Drug Information - 3 questions
- Pharmaceutics (Safely dosing medications) - 2 questions
Neurodevelopmental Disabilities Exam Articles (136)
Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a mitochondrial disease primarily affecting the nervous s ...
Aphasia is a term used to describe a disturbance in the ability to use symbols (written or spoken) to communicate information and is categorized in ...
Opisthotonus is defined as a dramatic abnormal posture due to spastic contraction of the extensor muscles of the neck, trunk, and lower extremities ...
Wyburn-Mason syndrome (WMS), also known as racemose angioma, is a congenital nonhereditary neurocutaneous syndrome or phakomato ...
Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome characterized by angiomas involving the face, choroid, and leptomeninges. The facial capil ...
Vitamins are vital components to every individual’s day to day chemical reactions and molecular processes. They are used as cofactors for rea ...
Arnold-Chiari, or simply Chiari malformation, is the name given to a group of deformities of the posterior fossa and hindbrain (cerebellum, pons, a ...
Schizencephaly is a rare congenital neuronal migration disorder characterized by the presence of a full-thickness cleft, lined with heterotopi ...
Tuberous sclerosis complex (TSC) is a genetic disorder that affects multiple systems. It is inherited in an autosomal dominant fashion and is chara ...
Basilar invagination is an abnormality at the craniovertebral junction, either congenital or degenerative, resulting in the odontoid prolapsing int ...
Kayser–Fleischer (KF) rings are a common ophthalmologic finding in patients with Wilson disease. Initially thought to be due to the accumulat ...
Fragile X syndrome (FXS), also called Martin-Bell syndrome, is a non-Mendelian trinucleotide repeat disorder. FXS is the most prevalent inheri ...
Down syndrome was first described by an English physician John Langdon Down in 1866, but its association with chromosome 21 was established almost ...
Arginase deficiency (argininemia) is an autosomal recessive metabolic disorder characterized by hyperammonemia secondary to arginine accumulation. ...
Michael J Labanowski MD Southeast Alabama Medical Center American Board of Sleep Disorders Medicine Dothan AL
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