Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Intro (0:35),

Selective IgA deficiency (1:35),

Bruton's agammaglobulinemia (3:32),

Transient hypogammaglobulinemia (4:52),

Hyper IgM syndrome (5:50),

Common variable immunodeficiency (CVID) (6:57),

Severe combined immunodeficiency (SCID) (8:22),

DiGeorge syndrome (11:03),

Ataxia telangiectasia (13:26),

Wiskott-Aldrich syndrome (14:59),

Hyper IgE syndrome (16:07),

Leukocyte adhesion deficiency (18:09),

Chediak-Higashi syndrome (19:16),

Chronic granulomatous disease (20:14),

Complement deficiencies (22:01),

Leukemia and lymphoma (23:45),

Secondary immunodeficiencies (25:30),

Practice questions (27:27)

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Intro (0:35),

Galactosemia (1:41),

Hereditary fructose intolerance (3:42),

Essential fructosuria (4:26),

Glycogen storage diseases (4:48),

Von Gierke disease (5:18),

Period Acid Schiff and Diastase test (PAS-D) (6:02),

Pompe disease (6:38),

Cori disease (7:46),

Andersen disease (8:21),

McArdle disease (9:01),

Phenylketonuria (11:10),

Alkaptonuria (13:01),

Maple syrup urine disease (14:19),

Homocystinuria (16:01),

Urea cycle disorders (17:40),

Fatty acid metabolism disorders (19:14),

Lysosomal storage diseases (20:30),

Tay-Sachs disease (20:58),

Niemann-Pick disease (22:07),

Gaucher disease (22:44),

Metachromatic leukodystrophy (23:39),

Krabbe disease (24:41),

Hurler disease and Hunter disease (25:41),

Fabry disease (26:33),

Lesch-Nyhan syndrome (27:31),

Adenosine deaminase deficiency (28:20),

Practice questions (28:47)

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Intro (0:35),

Infant neuro exam (1:42),

Infantile spasms (7:33),

Erb's palsy and Klumpke's palsy (9:24),

Primitive reflexes (10:34),

Head circumference (12:27),

Papilledema (15:05),

Increased ICP (16:22),

Cushing's triad (17:50),

Brain herniation (20:28),

Basic diagnostic and therapeutic strategies (22:35),

Birth asphyxia (26:07),

Hypoxic Ischemic Encephalopathy (HIE) (28:33),

Cerebral palsy (29:59),

Intracranial hemorrhage (31:28),

Hydrocephalus (38:57),

Cortical defects (42:53),

Neural tube defects (46:50),

Posterior fossa defects (51:03),

Cerebellar ataxia disorders (54:44),

Neonatal myasthenia gravis (57:32),

Muscular dystrophy (58:47),

Needle electromyography & nerve conduction studies (1:00:42),

Neurological infections (1:04:08),

Metabolic disorders (1:06:09),

Mitochondrial disorders (1:08:09),

Practice questions (1:09:09)

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Intro (0:35),

Potter sequence (1:45),

Renal agenesis (2:45),

Renal cysts (4:06),

Autosomal dominant polycystic kidney disease (ADPKD) (5:04),

Autosomal recessive polycystic kidney disease (ARPKD) (6:45),

MCKD and JNPH (8:03),

Tuberous sclerosis (8:24),

Von Hippel Lindau (9:02),

Horseshoe kidney (9:58),

Ureteropelvic junction obstructions (10:39),

Voiding cystourethrography (VCUG) (11:15),

Posterior urethral valves (11:26),

Vesicoureteral reflux (12:05),

Hypospadias (14:20),

Epispadias and bladder-exstrophy-epispadias-complex (BEEC) (15:15),

Prune Belly Syndrome (16:03),

Disorders of sexual development (16:41),

Ambiguous genitalia (17:44),

Embryology of sex differentiation (20:16),

Anti-Mullerian hormone (20:57),

Testosterone (21:24),

Dihydrotestosterone (21:55),

5a-reductase deficiency (22:09),

Androgen insensitivity syndrome (22:26),

Aromatase deficiency (23:34),

Congenital adrenal hyperplasia (24:30),

21-Hydroxylase deficiency (26:40),

Other causes of CAH (30:41),

Kallman syndrome (32:17),

Semil-Lemil-Opitz syndrome (32:58),

Practice questions (33:27)

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Intro (0:35),

Congenital GI defects overview (1:28),

Esophageal atresia and tracheoesophageal fistula (2:17),

VACTERL syndrome (3:44),

Hypertrophic pyloric stenosis (4:34),

Duodenal atresia and the "double bubble" sign (6:07),

Intestinal malrotation and midgut volvulus (6:57),

Annular pancreas (9:03),

Jejunal-ileal atresia (10:14),

Gastroschisis and omphalocele (11:15),

Duplication cysts (12:24),

Meckel's diverticulum (13:44),

Imperforate anus (14:57),

Hirschsprung disease (15:54),

Cystic fibrosis (16:45),

Congenital pulmonary airway malformation (24:07),

Pulmonary sequestration (25:13),

Congenital lobar emphysema (26:09),

Bronchogenic cysts (26:19),

Congenital diaphragmatic hernia (26:55),

Pulmonary hypoplasia (28:33),

Potter syndrome (28:44),

Scimitar syndrome (29:08),

Laryngomalacia (29:27),

Transient tachypnea of the newborn (30:07),

Neonatal respiratory distress syndrome (30:36),

Necrotizing enterocolitis (31:24),

Practice questions (32:04)

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Intro (0:35),

Fetal circulatory system (2:05),

Persistent fetal circulation (6:43),

Patent ductus arteriosus (8:07),

Differential cyanosis (8:45),

CCHD screening (9:29),

Common themes (10:44),

Non-cyanotic heart defects (13:31),

Ventricular septal defects (14:13),

Atrial septal defects (15:40),

Eisenmenger syndrome (16:33),

Aortic and pulmonary stenosis (17:47),

Coarctation of the aorta (18:47),

Double aortic arch (19:58),

Interrupted aortic arch (21:12),

Cyanotic heart defects (21:39),

Tetralogy of Fallot (23:44),

Transposition of the great arteries (28:08),

Hypoplastic left heart syndrome (29:52),

Persistent truncus arteriosus (31:14),

Partial and total anomalous pulmonary venous connection (33:06),

Scimitar syndrome (35:09),

Tricuspid and pulmonary atresia (36:08),

Prostaglandin E1 indications (36:36),

DiGeorge syndrome (38:13),

CHARGE syndrome (38:47),

Dextrocardia (39:11),

Situs inversus and total situs inversus (39:21),

Ebstein anomaly (40:09),

Noonan syndrome (40:39),

Marfan syndrome (40:57),

Turner syndrome (41:16),

Down syndrome (41:33),

Congenital heart blocks (43:08),

Practice questions (43:32)

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Aneuploidy, Robertsonian translocation, mosaicism, prenatal screening, physical exam findings, Down's syndrome, Edward's syndrome, Patau syndrome, Klinefelter syndrome, Turner syndrome, Triple X syndrome, XYY syndrome, Cri Du Chat syndrome, Wolf-Hirschhorn syndrome, Jacobsen and Paris-Troussaeu syndromes, Charcot-Marie-Tooth syndrome, Prader-Willi and Angelman syndromes, trinucleotide repeat disorders, Fragile X syndrome, Huntington Disease, Myotonic dystrophy Type I, spinocerebellar ataxia, and Friedrich ataxia.

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

TORCH, perinatal infections

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Intro (0:35),

Zygosity, chorionicity, and amnionicity (2:18),

Ultrasound findings (7:59),

Maternal complications (10:58),

Fetal complications (12:40),

Practice questions (16:32)

Q-BANK: https://www.patreon.com/highyieldfamilymedicine

Vitals (1:48),

General appearance (3:59),

Skin/neonatal rashes (4:35),

Head (12:18),

Face (19:53),

Eyes (20:20),

Ears (25:32),

Nose (26:31),

Mouth (27:06),

Neck (29:03),

Chest (30:29),

Lungs (31:13),

Heart (32:00),

Abdomen (33:35),

Genitourinary (35:09),

MSK, Neuro (42:21),

Practice questions (48:21)