Androgen Insensitivity Syndrome: Biology and Care
Androgen insensitivity syndrome (AIS) is an X-linked genetic condition where 46,XY individuals exhibit reduced or...
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Psychological Dictionary
28 results
Anatomical Age: Measuring Biological Maturation
Anatomical age is the objective developmental status of an organism's physical and skeletal structures evaluated...
October 7, 2026
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Dr. Mohammed Looti
Amsterdam Dwarfism: Clinical Profile
Amsterdam dwarf disease, clinically termed Cornelia de Lange syndrome (CdLS), is a rare genetic cohesinopathy...
October 7, 2026
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Dr. Mohammed Looti
AIS: Understanding Androgen Insensitivity
An authoritative academic guide to Androgen Insensitivity Syndrome (AIS), exploring its genetic causes, clinical subtypes,...
October 6, 2026
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Dr. Mohammed Looti
Adrenogenital Syndrome: Hormones and Development
An in-depth academic examination of adrenogenital syndrome, detailing its enzymatic mechanisms, clinical presentations, diagnostic frameworks,...
October 6, 2026
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Dr. Mohammed Looti
Adolescent Growth Spurt: Dynamics of Maturation
An exhaustive academic overview of the adolescent growth spurt, detailing its endocrine mechanisms, peak height...
October 6, 2026
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Dr. Mohammed Looti
Acute Otitis Media: Clinical Overview and Pathophysiology
A comprehensive academic dictionary entry and clinical review of acute otitis media (AOM), detailing its...
October 6, 2026
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Dr. Mohammed Looti
Acute Cerebellar Ataxia: Rapid Motor Decline
Acute cerebellar ataxia is a neurological condition marked by the sudden onset of gait instability,...
October 6, 2026
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Dr. Mohammed Looti
Acrodysostosis: Skeletal and Endocrine Rare Disease
Acrodysostosis is a rare genetic disorder characterized by severe skeletal dysplasia, brachydactyly, facial dysmorphism, and...
October 5, 2026
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Dr. Mohammed Looti
Acrocephaly: Understanding Tower Skull Deformity
Acrocephaly is a severe congenital craniofacial malformation characterized by a tall, tower-like, or pointed cranial...
October 5, 2026
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Dr. Mohammed Looti
Acrocephalosyndactyly: Genetics and Phenotype
Acrocephalosyndactyly is a group of rare genetic disorders characterized by craniosynostosis and syndactyly, primarily caused...
October 5, 2026
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Dr. Mohammed Looti
Acrocephalopolysyndactyly: Clinical Spectrum
Acrocephalopolysyndactyly is a rare genetic condition characterized by craniosynostosis, polysyndactyly, and systemic anomalies, primarily classified...
October 5, 2026
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Dr. Mohammed Looti