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 247 Multiple-choice 1st, 2nd, and 3rd order questions with four detailed teaching points linked to 133 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. 146 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 (247)
Our question bank for the Neurodevelopmental Disabilities Exam covers four Cognitive Difficulty Levels:
- Cardiovascular - 5 questions
- Connective Tissue - 1 questions
- Ears Nose and Throat - 5 questions
- Endocrine and Metabolic - 23 questions
- Eyes - 12 questions
- Gastrointestinal - 4 questions
- Genetics - 114 questions
- Genitourinary - 1 questions
- Growth and Development - 142 questions
- Infectious - 1 questions
- Integument - 18 questions
- Musculoskeletal - 48 questions
- Nervous - 236 questions
- Nutrition - 3 questions
- Obstetric - 7 questions
- Oncologic - 6 questions
- Psychiatric Mental Health - 36 questions
- Pulmonary - 1 questions
- Renal - 3 questions
- Surgery - 3 questions
- Toxicology - 2 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) - 3 questions
- Physiological Adaptation (Care Ill Patients) - 114 questions
- Psychosocial (Mental Health Patient/Family) - 20 questions
- Process (Analysis, Assess, Eval, Implement, Plan) - 137 questions
- Teaching/Learning (Promotes Behavior Change) - 2 questions
- Causes - 90 questions
- Classification - 37 questions
- Differential - 178 questions
- Epidemiology - 12 questions
- Evaluation Diagnostic Tests - 48 questions
- Evaluation Lab - 22 questions
- Evaluation Monitoring - 11 questions
- Evaluation Procedures - 22 questions
- Evaluation Radiologic - 94 questions
- Health Maint Prevention Public Health - 2 questions
- History Physical - 263 questions
- Legal - 1 questions
- Pathophysiology - 151 questions
- Patient Education - 6 questions
- Prognosis Complications - 137 questions
- Toxicology - 1 questions
- Treatment Medical - 31 questions
- Treatment Rehabilitation - 4 questions
- Treatment Surgical - 8 questions
- Healthcare Ethics - 1 questions
- Clinical Education - 3 questions
- Therapeutics (Drug treatment) - 2 questions
- Drug Information - 2 questions
- Pharmaceutics (Safely dosing medications) - 1 questions
Neurodevelopmental Disabilities Exam Articles (133)
Oxidation of fatty acids occurs in multiple regions of the cell within the human body; the mitochondria, in which only Beta-oxidation occurs; ...
Lesch Nyhan syndrome is an inborn disorder caused by a deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme, an enzyme of the ...
Hunter syndrome is a genetically associated lysosomal storage disorder due to the deficiency of the iduronate 2-sulfatase enzyme (IDS). It is an X- ...
Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a mitochondrial disease primarily affecting the nervous s ...
The septum pellucidum (meaning translucent wall in Latin - SP), also known as the ventricle of Sylvius, is a thin, triangular double membrane separ ...
Lysosomal storage diseases (LSDs) are a group of hereditary disorders that disrupt lysosomal function, specifically, enzymes involved in cell metab ...
Attention Deficit-Hyperactivity Disorder (ADHD) is a psychiatric condition that has long been recognized as affecting children's ability to fu ...
The atlantoaxial segment consists of the atlas (C1) and axis (C2) and forms a complex transitional structure bridging the occiput and cervical spin ...
Lennox-Gastaut syndrome (LGS) is a rare but severe form of childhood epilepsy that was first described by Dr. Henri Gastaut in Marseille, France in ...
Learning disabilities (LDs) refer to several disorders that may affect the acquisition, organization, retention, comprehension, or the use of both ...
Prader Willi syndrome (PWS) is a rare and complex genetic disease, with numerous implications on metabolic, endocrine, neurologic systems, with beh ...
Child development is a complex process that begins in the womb and continues until adulthood. It is influenced by biology and the environment, and ...
Myotonic dystrophy (DM) is considered a subgroup of myopathy and the most common type of muscular dystrophy that begins in adulthood. There are two ...
Michael J Labanowski MD Southeast Alabama Medical Center American Board of Sleep Disorders Medicine Dothan AL
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