Neurocognitive Deficits Archives

Death

Subacute Sclerosing Panencephalitis

What is Subacute Sclerosing Panencephalitis? Subacute Sclerosing Panencephalitis, also known as SSPE, is a rare but …

Angiomyolipomas

Tuberous Sclerosis

What is Tuberous Sclerosis? Tuberous sclerosis complex (TSC) is a genetic condition passed down through families. …

Congenital Heart Disease

Alagille Syndrome

What is Alagille Syndrome? Alagille syndrome, also known as Alagille-Watson syndrome or some other names, is …

Headache

Postconcussive Syndrome

What is Postconcussive Syndrome? Traumatic brain injury (TBI), a condition that can happen to anyone at …

Cafe-au-lait Macules

Neurofibromatosis Type 1 (Von Recklinghausen Disease)

What is Neurofibromatosis Type 1 (Von Recklinghausen Disease)? Neurofibromatosis type 1 (NF-1), also known as Von …

Further Neurocognitive Deficits Topics

45,X with Mosaicism Albright Hereditary Osteodystrophy Alkaptonuria alpha-dystroglycanopathies Becker Dystrophy Beckwith-Wiedemann Syndrome Bethlehem Dystrophy Birt-Hogg-Dube syndrome BRCA1 and BRCA2 Cayler Cardio-Facial Syndrome Channelopathy Congenital Heart Disease Corneal Dystrophy Cornelia de Lange Syndrome Cri Du Chat Syndrome Crigler-Najjar Cystic Fibrosis De Barsy Syndrome DiGeorge Syndrome Down Syndrome Duchenne Muscular Dystrophy Ehlers Danlos Syndrome Enzyme Deficiencies Familial Adenomatous Polyposis Familial Aldosteronism Familial Combined Hyperlipidemia Familial Htpertriglyceridemia Familial Hypercholesterolemia Familial Hypoalphalipoproteinemia Familial Hypocalciuric Hypercalcemia Fragile X Syndrome Friedreich Ataxia Fuchs Endothelial Corneal Dystrophy Gardenr Syndrome Genetic Kidney Disease Gilbert Syndrome Gorlin-Goltz Syndrome Growth Failure Hereditary Angioedema Hereditary Ataxia Homocystinuria Human Leukocyte Antigen B27 Hypoxanthine-Guanine Phosphoribosyltransferase (HPRT) Enzyme Deficiency Inborn Errors of Metabolism Infantile Refsum Disease (IRD) Kartagener Syndrome Lesch-Nyhan Syndrome Liddle Syndrome Liver Disease Lucy-Driscoll Syndrome Lynch Syndrome Lysosomal Storage Disease Lysosomal Storage Diseases Marfan Syndrome Metabolic Myopathy Mitochondrial Disorders Monosomy X (45,XO) Multiple Endocrine Neoplasia 1 Muscular Dystrophy Myotonic Dystrophy Neonatal Adrenoleukodystrophy (NALD) Neurocognitive Deficits Ophthalmologic Abnormalities Plummer-Vinson Syndrome Pseudohypoparathyroidism Respiratory Diseases Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1) Sex Chromosome Trisomy Situs Inversus Totalis Skeletal Anomalies Spinocerebellar Ataxia Tuberous Sclerosis Turcot Syndrome Von Hippel-Lindau Syndrome X-Linked Disorders XYY Zellweger Syndrome

Acanthocytes

Neuroacanthocytosis

Published: August 28, 2024

What is Neuroacanthocytosis? Neuroacanthocytosis is a term for a few hereditary disorders, which leads to unusually …

28 Aug 24

Genetic Disorder

Metachromatic Leukodystrophy

Published: August 21, 2024

What is Metachromatic Leukodystrophy? Lysosomal storage diseases (LSDs) are a set of inherited diseases that interfere …

21 Aug 24

Alzheimer Disease

Major Neurocognitive Disorder (Dementia)

Published: August 16, 2024

What is Major Neurocognitive Disorder (Dementia)? The term dementia has undergone some changes in medical terminology. …

16 Aug 24

Dementia

HIV Encephalitis (HIV-associated neurological disorder (HAND)

Published: August 9, 2024

What is HIV Encephalitis (HIV-associated neurological disorder (HAND)? HIV encephalitis, sometimes referred to as HIV-associated neurological …

9 Aug 24

Advanced Age

HIV Neurocognitive Disorders

Published: August 9, 2024

What is HIV Neurocognitive Disorders? People infected with human immunodeficiency virus (HIV, a virus that attacks …

9 Aug 24

Aphasia

Primary Central Nervous System Vasculitis

Published: August 8, 2024

What is Primary Central Nervous System Vasculitis? Primary angiitis of the central nervous system (PACNS) is …

8 Aug 24

Macular Degeneration

Charles Bonnet Syndrome

Published: August 3, 2024

What is Charles Bonnet Syndrome? Charles Bonnet syndrome (CBS) is a condition where a person experiences …

3 Aug 24

Coma

Hyperbaric Treatment of Carbon Monoxide Toxicity

Published: July 30, 2024

What is Hyperbaric Treatment of Carbon Monoxide Toxicity? Carbon monoxide (CO) is a harmful gas that …

30 Jul 24

Behavioral

Repetitive Head Injury Syndrome

Published: July 30, 2024

What is Repetitive Head Injury Syndrome? Chronic Traumatic Encephalopathy (CTE), originally known as “punch drunk” syndrome, …

30 Jul 24

Further Neurocognitive Deficits Topics

45,X with Mosaicism

Albright Hereditary Osteodystrophy

Alkaptonuria

alpha-dystroglycanopathies

Becker Dystrophy

Beckwith-Wiedemann Syndrome

Bethlehem Dystrophy

Articles

Further Neurocognitive Deficits Topics

45,X with Mosaicism

Albright Hereditary Osteodystrophy

Alkaptonuria

alpha-dystroglycanopathies

Becker Dystrophy

Beckwith-Wiedemann Syndrome

Bethlehem Dystrophy

Birt-Hogg-Dube syndrome

BRCA1 and BRCA2

Cayler Cardio-Facial Syndrome

Channelopathy

Congenital Heart Disease

Corneal Dystrophy

Cornelia de Lange Syndrome

Cri Du Chat Syndrome

Crigler-Najjar

Cystic Fibrosis

De Barsy Syndrome

DiGeorge Syndrome

Down Syndrome

Duchenne Muscular Dystrophy

Ehlers Danlos Syndrome

Enzyme Deficiencies

Familial Adenomatous Polyposis

Familial Aldosteronism

Familial Combined Hyperlipidemia

Familial Htpertriglyceridemia

Familial Hypercholesterolemia

Familial Hypoalphalipoproteinemia

Familial Hypocalciuric Hypercalcemia

Fragile X Syndrome

Friedreich Ataxia

Fuchs Endothelial Corneal Dystrophy

Gardenr Syndrome

Genetic Kidney Disease

Gilbert Syndrome

Gorlin-Goltz Syndrome

Growth Failure

Hereditary Angioedema

Hereditary Ataxia

Homocystinuria

Human Leukocyte Antigen B27

Hypoxanthine-Guanine Phosphoribosyltransferase (HPRT) Enzyme Deficiency

Inborn Errors of Metabolism

Infantile Refsum Disease (IRD)

Kartagener Syndrome

Lesch-Nyhan Syndrome

Liddle Syndrome

Liver Disease

Lucy-Driscoll Syndrome

Lynch Syndrome

Lysosomal Storage Disease

Lysosomal Storage Diseases

Marfan Syndrome

Metabolic Myopathy

Mitochondrial Disorders

Monosomy X (45,XO)

Multiple Endocrine Neoplasia 1

Muscular Dystrophy

Myotonic Dystrophy

Neonatal Adrenoleukodystrophy (NALD)

Neurocognitive Deficits

Ophthalmologic Abnormalities

Plummer-Vinson Syndrome

Pseudohypoparathyroidism

Respiratory Diseases

Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1)

Sex Chromosome Trisomy

Situs Inversus Totalis

Skeletal Anomalies

Spinocerebellar Ataxia

Tuberous Sclerosis

Turcot Syndrome

Von Hippel-Lindau Syndrome

X-Linked Disorders

XYY

Zellweger Syndrome

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