Pulmonary hypoplasia

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Pulmonary hypoplasia

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Vascular tumors
DNA alkylating medications
Pediatric bone tumors: Clinical
Pediatric gastrointestinal bleeding: Clinical
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Fragile X syndrome
Huntington disease
Myotonic dystrophy
Friedreich ataxia
Klinefelter syndrome
Angelman syndrome
Prader-Willi syndrome
Cri du chat syndrome
Williams syndrome
Alport syndrome
Marfan syndrome
von Hippel-Lindau disease
Newborn management: Clinical
Atypical antidepressants
Acid reducing medications
Adrenergic antagonists: Alpha blockers
Cell wall synthesis inhibitors: Penicillins
Protein synthesis inhibitors: Aminoglycosides
Herpesvirus medications
Stevens-Johnson syndrome
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Nonbenzodiazepine anticonvulsants
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Coagulation (secondary hemostasis)
Patau syndrome (Trisomy 13)
Hypothyroidism medications
Spina bifida
Persistent truncus arteriosus
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DNA synthesis inhibitors: Fluoroquinolones
Miscellaneous protein synthesis inhibitors
Ventricular septal defect
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Endocarditis: Pathology review
Infective endocarditis: Clinical
Endocarditis
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Fatty acid oxidation
Echinocandins
Haemophilus ducreyi (Chancroid)
Urinary tract infections: Clinical
Movement of water between body compartments
Typical antipsychotics
Cholinomimetics: Indirect agonists (anticholinesterases)
Positive inotropic medications
cGMP mediated smooth muscle vasodilators
Aortic valve disease
Familial hypercholesterolemia
Cardiovascular system anatomy and physiology
Hemophilia
Antimetabolites for cancer treatment
Complement system
Topoisomerase inhibitors
Eye conditions: Inflammation, infections and trauma: Pathology review
Meningitis
Muscle spindles and golgi tendon organs
Ascending and descending spinal tracts
Trigeminal neuralgia
Hypokinetic movement disorders: Clinical
Cerebellum
Basal ganglia: Direct and indirect pathway of movement
Anatomy of the olfactory (CN I) and optic (CN II) nerves
Photoreception
Cholinergic receptors
Hemianopsia
Nervous system anatomy and physiology
Peripheral nervous system histology
Major depressive disorder
Congenital adrenal hyperplasia
Urinary incontinence: Pathology review
Acute respiratory distress syndrome
Anatomy of the abdominal viscera: Large intestine
Congenital gastrointestinal disorders: Pathology review
Somatosensory pathways
Jaundice: Pathology review
Influenza virus
Alveolar surface tension and surfactant
Abnormal heart sounds
Fetal circulation
Total anomalous pulmonary venous return
Anatomy of the anterolateral abdominal wall
Anthelmintic medications
Hernias: Clinical
Cerebrospinal fluid
Vestibulo-ocular reflex and nystagmus
Night terrors
Cannabis use disorder
Sympathetic nervous system
Cocaine use disorder
Complement deficiency
Brown-Sequard Syndrome
Bacillus cereus (Food poisoning)
Deep vein thrombosis and pulmonary embolism: Pathology review
Spinal muscular atrophy
Sleep disorders: Clinical
Lung cancer
Adult brain tumors
Polycystic kidney disease
Pulmonary hypoplasia
Sensitivity and specificity
Developmental milestones: Clinical
Lymphatic system anatomy and physiology
Shaken baby syndrome
Shigella
Beckwith-Wiedemann syndrome
Iron deficiency anemia
Vessels and nerves of the gluteal region and posterior thigh
Emotion
Antidiarrheals
Vascular dementia
Aspergillus fumigatus
Cryptococcus neoformans
Trichuris trichiura (Whipworm)
Multiple endocrine neoplasia
Growth hormone deficiency
Growth and development
Cartilage structure and growth
Pituitary adenoma
Coxsackievirus
Pediatric brain tumors
Gallbladder disorders: Pathology review
Gallbladder disorders: Clinical
Extracellular matrix
Ischemia
Vitamin K deficiency
Jaundice: Clinical
Prebiotics and probiotics
Nucleotide metabolism
Immune thrombocytopenia
Hyperlipidemia
Hypertriglyceridemia
Respiratory syncytial virus
Megaloblastic anemia
Fatty acid synthesis
Multiple myeloma
Waldenstrom macroglobulinemia
Systemic lupus erythematosus
Hypercalcemia
Strongyloides stercoralis
Polycythemia vera (NORD)
Hypokalemia
Metabolic alkalosis
Paracetamol toxicity
Chronic kidney disease
Myelofibrosis (NORD)
Age-related macular degeneration
Myeloproliferative neoplasms: Clinical
Metaplasia and dysplasia
Blood brain barrier
Epidural abscess
Cystinosis
Fat-soluble vitamin deficiency and toxicity: Pathology review
Zinc deficiency and protein-energy malnutrition: Pathology review
Water-soluble vitamin deficiency and toxicity: B1-B7: Pathology review
Kidney stones
Pasteurella multocida
Mitosis and meiosis
Haemophilus influenzae
Escherichia coli
Cell membrane
Otitis externa
Primary ciliary dyskinesia
Rheumatic heart disease
Sjogren syndrome: Clinical
Attention deficit hyperactivity disorder
Neonatal ICU conditions: Clinical
Oncogenes and tumor suppressor genes
Muscular system anatomy and physiology
Polycystic ovary syndrome
Azoles
Brain abscess
Disease causality
Entamoeba histolytica (Amebiasis)
Bone tumors
Pediatric infectious rashes: Clinical
Lower back pain: Clinical
Antiphospholipid syndrome
Adrenal insufficiency: Pathology review
Dementia and delirium: Clinical
Eczematous rashes: Clinical
Pulmonary embolism
Syncope: Clinical
Pharyngeal arches, pouches, and clefts
Uterine disorders: Pathology review
Distal convoluted tubule
Antidiuretic hormone
Adrenal hormone synthesis inhibitors
Idiopathic intracranial hypertension
Clinical Skills: Body Temperature Assessment
Toxidromes: Clinical
Anxiolytics and sedative-hypnotics: Nursing pharmacology
Abuse, mistreatment, and neglect
Sensory system: Eye and ear disorders
Vaccinations: Clinical
Anatomy of the orbit
Clinical Skills: High-frequency oscillatory ventilation (HFOV)
Anxiety disorders: Clinical
Primary adrenal insufficiency
Hodgkin lymphoma
Sympatholytics: Alpha-2 agonists
Antidepressants - SSRIs and SNRIs: Nursing pharmacology
Antimetabolites for cancer treatment
Pediatric upper airway conditions: Clinical

Key Takeaways

Pulmonary hypoplasia is a congenital condition in which the lungs are underdeveloped, resulting in an abnormally low number or size of bronchopulmonary segments or alveoli and a reduced lung capacity. Symptoms of pulmonary hypoplasia include shortness of breath, rapid breathing, and difficulty feeding. Treatment for pulmonary hypoplasia involves providing supplemental oxygen or using a mechanical ventilator to help the baby breathe. In severe cases, a lung transplant may be necessary.