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developmental anomalies
How are Developmental Anomalies Classified?
Developmental anomalies can be classified based on their occurrence in different organ systems or tissues. Common classifications include:
Central nervous system anomalies (e.g.,
spina bifida
, anencephaly)
Cardiovascular anomalies (e.g.,
tetralogy of Fallot
, atrial septal defect)
Musculoskeletal anomalies (e.g.,
clubfoot
, polydactyly)
Gastrointestinal anomalies (e.g.,
cleft palate
, esophageal atresia)
Genitourinary anomalies (e.g., hypospadias, renal agenesis)
Frequently asked queries:
What are Developmental Anomalies?
What Causes Developmental Anomalies?
How are Developmental Anomalies Classified?
What are Some Common Developmental Anomalies and Their Histological Features?
How are Developmental Anomalies Diagnosed?
What is the Role of Histology in Understanding Developmental Anomalies?
Can Developmental Anomalies be Prevented?
What are the Treatment Options for Developmental Anomalies?
How Is Chemotaxis Studied in Histology?
Why Use Knockout Models?
How is Transferrin Detected in Histological Samples?
How do Cox Negative Fibers Relate to Mitochondrial Myopathies?
What Are the Implications of Abnormal Morphogenesis?
How is Ultrasound used in conjunction with Histology?
How Do Histological Changes Inform Clinical Management of Diabetes?
Why Might Overtime be Necessary in Histology?
Why is Ferritin Storage Important in Histology?
What Can Be Diagnosed from a Renal Biopsy?
What Are the Common Sources of Power Surges?
How is RNA Polymerase III Regulated?
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