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Learning disability

Paediatrics Sara

Paediatrics Sara

Seizures: Pathology review
Seizures: Clinical
Seizures and epilepsy
Early infantile epileptic encephalopathy (NORD)
Anticonvulsants and anxiolytics: Benzodiazepines
Nonbenzodiazepine anticonvulsants
Febrile seizure
Meningitis
Meningitis, encephalitis and brain abscesses: Clinical
Neonatal meningitis
Neisseria meningitidis
Central nervous system infections: Pathology review
Disorders of consciousness: Clinical
Cerebral palsy
Cerebral circulation
Neurodevelopmental disorders: Clinical
Pediatric brain tumors
Spina bifida
Congenital disorders: Clinical
Developmental milestones: Clinical
Precocious and delayed puberty: Clinical
Constitutional growth delay
Delayed puberty
Learning disability
Neurofibromatosis
ADHD: Information for patients and families (The Primary School)
Disorders of sex chromosomes: Pathology review
Asthma: Clinical
Asthma
Asthma: Information for patients and families (The Primary School)
Respiratory syncytial virus
Influenza virus
Pediatric lower airway conditions: Clinical
Human parainfluenza viruses
Pneumonia
Moraxella catarrhalis
Pneumonia: Pathology review
Knowledge Shot: What over-the-counter medicine works best at kicking the cough of the common cold and bronchitis
Bronchiectasis
Corynebacterium diphtheriae (Diphtheria)
Croup
Pediatric upper airway conditions: Clinical
Clinical Skills: Using a metered-dose inhaler
Bacterial epiglottitis
Congenital pulmonary airway malformation
Upper respiratory tract infection
Neonatal respiratory distress syndrome
Acute respiratory distress syndrome
Acute respiratory distress syndrome: Clinical
Metabolic and respiratory alkalosis: Clinical
Shock: Clinical
Pediatric vomiting: Clinical
Shock
Pediatric allergies: Clinical
Dengue virus
Yellow fever virus
Zika virus
West Nile Virus Infection
Leptospira
Fever of unknown origin: Clinical
Salmonella typhi (typhoid fever)
Salmonella (non-typhoidal)
Salmonellosis
Epstein-Barr virus (Infectious mononucleosis)
Pediatric ear, nose, and throat conditions: Clinical
Lymphomas: Pathology review
Non-Hodgkin lymphoma
Hodgkin lymphoma
Bordetella pertussis (Whooping cough)
Vaccinations: Clinical
Vaccinations
Clostridium tetani (Tetanus)
Kawasaki disease
Kawasaki disease: Clinical
Vasculitis: Clinical
Vasculitis: Pathology review
Pediatric infectious rashes: Clinical
Diarrhea: Clinical
Gastroenteritis
Vibrio cholerae (Cholera)
Rotavirus
Norovirus
Inflammatory bowel disease: Pathology review
Campylobacter jejuni
Listeria monocytogenes
Tropical sprue
Abdominal pain: Clinical
Intussusception
Congenital gastrointestinal disorders: Pathology review
Diverticular disease: Clinical
Bowel obstruction: Clinical
Pediatric gastrointestinal bleeding: Clinical
Malabsorption syndromes: Pathology review
Nephritic and nephrotic syndromes: Clinical
Nephrotic syndromes: Pathology review
Membranoproliferative glomerulonephritis
Lupus nephritis
Nephritic syndromes: Pathology review
Focal segmental glomerulosclerosis (NORD)
Minimal change disease
Membranous nephropathy
Chronic kidney disease: Clinical
Acute kidney injury: Clinical
Horseshoe kidney
Urinary tract infections (UTIs): Nursing process (ADPIE)
Urinary tract infections: Clinical
Urinary tract infections: Pathology review
Lower urinary tract infection
Urinary incontinence: Pathology review
Acute pyelonephritis
Pediatric urological conditions: Clinical
Postoperative evaluation: Clinical
Chronic pyelonephritis
Kidney stones: Clinical
Proteus mirabilis
Posterior urethral valves
Bladder exstrophy
Hydronephrosis
Growth hormone deficiency
Growth and development
Diabetes mellitus: Pathology review
Diabetes mellitus: Clinical
Hyperkalemia: Clinical
Metabolic acidosis
Thyroid nodules and thyroid cancer: Clinical
Thyroid nodules and thyroid cancer: Pathology review
Thyroid cancer
Hashimoto thyroiditis
Thyroid storm
Thyroid hormones
Hypothyroidism and thyroiditis: Clinical
Thyroid eye disease (NORD)
Thyroid and parathyroid gland histology
Anatomy of the thyroid and parathyroid glands
Hyperthyroidism: Clinical
Hyperthyroidism: Pathology review
Hypothyroidism: Pathology review
Hypothyroidism
Adrenal masses: Pathology review
Primary adrenal insufficiency
Adrenal masses and tumors: Clinical
Congenital adrenal hyperplasia
Adrenal cortical carcinoma
Adrenal insufficiency: Pathology review
Adrenal insufficiency: Clinical
Congenital adrenal hyperplasia: Clinical
Eczematous rashes: Clinical
Atopic dermatitis
Contact dermatitis
Seborrhoeic dermatitis
Blistering skin disorders: Clinical
Papulosquamous and inflammatory skin disorders: Pathology review
Papulosquamous skin disorders: Clinical
Benign hyperpigmented skin lesions: Clinical
Vesiculobullous and desquamating skin disorders: Pathology review
Staphylococcus epidermidis
Measles virus
Appendicitis: Clinical
Congenital TORCH infections: Pathology review
Mumps virus
Human herpesvirus 6 (Roseola)
Pityriasis rosea
Human herpesvirus 8 (Kaposi sarcoma)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Streptococcus pyogenes (Group A Strep)
Rheumatic heart disease
Varicella zoster virus
Vasculitis
Rapidly progressive glomerulonephritis
Anemia: Clinical
Anemia of chronic disease
Chronic leukemia
Leukemias: Pathology review
Leukemia: Clinical
Acute leukemia
Myeloproliferative neoplasms: Clinical
Bone tumors
Pancoast tumor
Nephroblastoma (Wilms tumor)
Pediatric brain tumors: Pathology review
Stevens-Johnson syndrome
Immune thrombocytopenia
Thrombocytopenia: Clinical
Platelet disorders: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Impetigo
Osteogenesis imperfecta
Imperforate anus
Pediatric orthopedic conditions: Clinical
Slipped capital femoral epiphysis
Femoral hernia
Muscular dystrophy
Muscle weakness: Clinical
Congenital heart defects: Clinical
Cyanotic congenital heart defects: Pathology review
Acyanotic congenital heart defects: Pathology review
Valvular heart disease: Clinical
Valvular heart disease: Pathology review
Congenital syphilis
Congenital rubella syndrome
Congenital toxoplasmosis
Infective endocarditis: Clinical
Endocarditis
Endocarditis: Pathology review
Bacillus cereus (Food poisoning)
Streptococcus viridans
Klebsiella pneumoniae
Enterococcus
Restrictive cardiomyopathy
Neonatal jaundice: Clinical
Jaundice
Jaundice: Pathology review
Jaundice: Clinical
Neonatal sepsis
Neonatal ICU conditions: Clinical
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Rett syndrome
Reye syndrome
Conn syndrome
Marfan syndrome
Brugada syndrome
Dressler syndrome
Anatomy clinical correlates: Thoracic wall
Neonatal hepatitis
Apnea of prematurity
Fragile X syndrome
Newborn management: Clinical
Sudden infant death syndrome
BRUE, ALTE, and SIDS: Clinical
Shaken baby syndrome
Coarctation of the aorta
Tay-Sachs disease (NORD)
Intestinal atresia
Choanal atresia
Autosomal trisomies: Pathology review
Pyloric stenosis
Aqueductal stenosis
Pediatric constipation: Clinical
Pediatric ophthalmological conditions: Clinical
Pediatric bone and joint infections: Clinical
Skin and soft tissue infections: Clinical
Perinatal infections: Clinical
Disorders of amino acid metabolism: Pathology review
Immunodeficiencies: Clinical
Child abuse: Clinical
Sickle cell disease: Clinical
Cystic fibrosis: Clinical
Congenital cytomegalovirus (NORD)
Delirium

Transcript

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Content Reviewers

The DSM-5 defines specific learning disorders as a set of disorders that relate to having difficulty learning and developing certain skills for at least 6 months.

First, there’s dyslexia, which is difficulty with reading, then there’s dysgraphia, which is difficulty with writing, and finally there’s dyscalculia, which is difficulty with mathematics.

People can have difficulty with just one of those activities, but they can also have problems in all three areas.

These disorders are considered specific learning disorders because they don’t stem from another condition like an intellectual disorder or a global developmental delay, and they aren’t due to an obvious environmental cause like not being taught how to read, write, or do math.

Learning disorders are usually diagnosed during the school-aged years, when a child’s skill can be assessed and is found to fall significantly below the average of other children in their age group.

Dyslexia affects both oral and written communication throughout an individual’s life.

People with dyslexia often have trouble identifying letters or words, and this can result in slow, inaccurate, and effortful reading.

This often becomes obvious when a person with dyslexia is reading aloud, because they might have to hesitate or guess at words, and they might end up reading without normal intonation or expression.

Dyslexia can also cause difficulty with spelling because a person might add or omit letters by mistake.

Having to go through all of this extra effort with reading means that people with dyslexia might also have a hard time understanding what they’ve read, missing the deeper meaning of a passage, forgetting the correct sequence of events, or being unable to make inferences about what they’ve read.

Dysgraphia describes having trouble with writing: specifically, poor spelling and difficulty with grammar.

People with dysgraphia often have poor handwriting, even though they don’t have trouble with other fine motor skills, like, for example, using tweezers.

They might mix print and cursive writing, or might misuse upper and lowercase letters; as a result, their writing is often slow and labored, causing them to get writing fatigue.

Dysgraphia can also involve more global writing problems like having difficulty putting thoughts down on paper, or thinking and writing at the same time, which, as you might guess, leads to writing that lacks clarity and cohesion.

Finally, there’s dyscalculia.