Dictionary
Agenesis: Developmental Absences in Anatomy
Agenesis is the complete congenital absence of an organ or tissue resulting from the total...
Medical Genetics
24 results
Dictionary
AFP: Clinical Marker and Fetal Protein
Alpha-fetoprotein (AFP) is a critical oncofetal glycoprotein synthesized during embryonic development that serves as a...
October 6, 2026
•
Dr. Mohammed Looti
Dictionary
Adult Progeria: Decoding Werner Syndrome
Adult progeria, or Werner syndrome, is an ultra-rare autosomal recessive disorder caused by WRN gene...
October 6, 2026
•
Dr. Mohammed Looti
Dictionary
Adrenogenital Syndrome: Hormones and Development
An in-depth academic examination of adrenogenital syndrome, detailing its enzymatic mechanisms, clinical presentations, diagnostic frameworks,...
October 6, 2026
•
Dr. Mohammed Looti
Dictionary
Adrenal Hyperplasia: Clinical Spectrum and Genetics
Adrenal hyperplasia is a non-neoplastic proliferation of the adrenal cortex driven by enzymatic defects in...
October 6, 2026
•
Dr. Mohammed Looti
Dictionary
Acromicria: Clinical Genetics and Pathology
Acromicria is a dysmorphological and clinical sign denoting disproportionate smallness of the distal extremities (hands,...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Acrodysostosis: Skeletal and Endocrine Rare Disease
Acrodysostosis is a rare genetic disorder characterized by severe skeletal dysplasia, brachydactyly, facial dysmorphism, and...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Acrocephalosyndactyly: Genetics and Phenotype
Acrocephalosyndactyly is a group of rare genetic disorders characterized by craniosynostosis and syndactyly, primarily caused...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Acrocephalopolysyndactyly: Clinical Spectrum
Acrocephalopolysyndactyly is a rare genetic condition characterized by craniosynostosis, polysyndactyly, and systemic anomalies, primarily classified...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Achondroplasia: Genetic Insights & Care
Explore an academic overview of achondroplasia, detailing its FGFR3 genetic basis, molecular pathophysiology, clinical features,...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Achiria: Congenital Absence of the Hands
Achiria is a rare congenital anomaly marked by the complete absence of one or both...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Abiotrophy: The Genetics of Premature Cellular Decay
A comprehensive scholarly analysis of abiotrophy, covering its historical formulation by Sir William Gowers, cellular...
October 5, 2026
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Dr. Mohammed Looti