BRAIN AND TISSUE BANK FOR DEVELOPMENTAL DISORDERS
Department of Pediatrics, Room 10-035 BRB
University of Maryland, Baltimore
655 W. Baltimore Street
Baltimore, MD 21201
(410)-706-1755 (800)-847-1539 FAX: (410)-706-0020
e-mail: btbumab@umaryland.edu
in contract to:
THE NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT
NATIONAL INSTITUTES OF HEALTH
List of Disorders
(* signifies Surgical Tissue)
Acardia
Achondrogenesis, Type II
Achondroplasia
Acrania
Acute Endocarditis
Adrenoleukodystrophy
ALD, X-linked, Adult Cerebral
ALD, X-linked, AMN, Cerebral
ALD, X-linked, AMN, Cerebral Status Unknown
ALD, X-linked, AMN, Pure
ALD, X-linked, Carrier
ALD, X-linked, Childhood Cerebral
Adrenoleukodystrophy / Adrenomyeloneuropathy
Adrenomyeloneuropathy
Agensis of Corpus Callosum
Aicardi-Goutieres Syndrome
Aicardi-Goutieres Syndrome*
Alexander Disease
Alpers Disease
Alpers-Huttenlocher Syndrome
Alzheimer's Disease
Alzheimer's Disease, Early Onset
Alzheimer's Disease (see Chromosomal Disorder, Trisomy 21)
Alzheimer's Disease, Lewy Body Variant
Alzheimer's Disease, Lewy Body Variant / Schizophrenia
Alzheimer's Disease, Type II Astrocytosis
Alzheimer's Disease / Parkinson's Disease
Alzheimer's Disease-like, Mild
Amniotic Band Syndrome
Amyotrophic Lateral Sclerosis
Anencephaly
Angelman Syndrome
Anoxic-Ischemic Encephalopathy
Anoxic-Ischemic Encephalopathy, Acute
Anoxic-Ischemic Encephalopathy / Biliary Cirrhosis
Anoxic-Ischemic Encephalopathy / Periventricular Leukomalacia
Anoxic-Ischemic Injury, diffuse, old*
Aqueductal Atresia / Encephalocele / Hydrocephalus
Aqueductal Atresia / Hydrocephalus
Aqueductal Stenosis / Hydrocephalus
Arnold Chiari Malformation
Arthrogryposis
Astrocytoma Grade III
Ataxia
Ataxia Telangiectasia
Ataxia, Friedreich's
Atrophy, Brain
Attention Deficit Disorder
Autism
Autism / ALS
Autism / Mental Retardation
Autism / Rett Syndrome, R/O*
Autism / Seizure Disorder
Autism Relative (control)
Autism Related, Pervasive Developmental Disorder
Autism, Suspected
Autism, Unaffected Relative & Glioblastoma Multiforme
Autism, Unrelated Relative
AV Canal Defect and Omphalocele
Barth's Syndrome
Binswanger Syndrome
Body-Wall Complex
Brain Mets / Spine Mets
Branchio-Oto-Renal Syndrome
Carbamyl Phosphate Synthetase I Deficiency
Carbohydrate Glycoprotein Deficiency Syndrome
Cardia Fibroelastosis
Cardiac Anomalies
Carnitine Deficiency
Caudal Regression Syndrome
Cavernous Hemangioma
Cerebellar Degeneration
Cerebral Edema of Unknown Etiology
Cerebral Occular Facial Syndrome
Cerebral Palsy
Cerebral Palsy / Encephalopathy, Hepatic
Cerebral Palsy / Hydrocephalus
Cerebral Palsy / Mitochondrial Disorder, probable*
Cerebral Palsy / Parkinson's Disease
Charcot-Marie-Tooth Syndrome
CHARGE Association
Chondroplasia Punctata
Chondroplasia Punctata, Rhizomelic / Alzheimer's Disease
Choroid Plexus Angioma / Subarachnoid Hemorrhage
Chromosomal Disorder, 17, Ring Mosaic
Chromosomal Disorder, 45,X
Chromosomal Disorder, 45X/46XY
Chromosomal Disorder, 46, XX, 5q+
Chromosomal Disorder, 4p-Syndrome
Chromosomal Disorder, Balanced Translocation 6, 11
Chromosomal Disorder, Deletion, Chromosome 11
Chromosomal Disorder, Deletion, Chromosome 12
Chromosomal Disorder, Dup X, q22.3,q26 / Pelizaeus Merzbacher Disease
Chromosomal Disorder, Inversion Duplication 8
Chromosomal Disorder, Klinefelter's, (47,XXY)
Chromosomal Disorder, Other
Chromosomal Disorder, Partial Trisomy 19 / Partial Monosomy 6
Chromosomal Disorder, Ring Chromosome 6
Chromosomal Disorder, Ring Chromosome 9, Mosaic
Chromosomal Disorder, Ring Chromosome 21, Mosaic
Chromosomal Disorder, Translocation denovo 4;12
Chromosomal Disorder, Triple X Chromosome Anomaly
Chromosomal Disorder, Triploidy
Chromosomal Disorder, Triploidy (69 XXX)
Chromosomal Disorder, Trisomy 1
Chromosomal Disorder, Trisomy 7
Chromosomal Disorder, Trisomy 9
Chromosomal Disorder, Trisomy 13
Chromosomal Disorder, Trisomy 13-15
Chromosomal Disorder, Trisomy 15
Chromosomal Disorder, Trisomy 15, Mosaic
Chromosomal Disorder, Trisomy 16
Chromosomal Disorder, Trisomy 17
Chromosomal Disorder, Trisomy 18
Chromosomal Disorder, Trisomy 21
Chromosomal Disorder, Trisomy 21 / Alzheimer's Disease
Chromosomal Disorder, Trisomy 22
Chromosomal Disorder, Trisomy X
Chromosomal Disorder, X X X X Y Syndrome
Chromosomal Disorder, Unbalanced Translocation
Chronic Meningoencephalitis
Citrullinemia
Cockayne Syndrome
Congenital Abnormalities (Normal Brain)
Congenital Defects, Asplenic
Congenital Fibrosarcoma
Congenital Heart Defect
Congenital Hypotonia
Congenital Nephrosis, Suspected
COPD
Control
Control (Twins)
Control*
Cornelia de Lange Syndrome
Cornelia de Lange Syndrome / Mental Retardation
Cortical Basal Ganglia Degeneration
Cystic Fibrosis
Cystic Hygroma
Dandy-Walker Malformation
Dandy-Walker Malformation*
Dementia
Dementia, Multi-infarct Type
Depression
Dermatomyositis
Diabetic Ketoacidosis
Diaphragmatic Hernia
Dysautonomia, Familial
Dysmorphic Syndrome
Dysmorphology Syndrome
Dystonia
Dystonia / Ataxia
Dystonia / Meige Syndrome
Dystonia Related, Familial Tremor, Dysphonia
Dystonia, Acquired
Dystonia, Blepharospasm
Dystonia, Blepharospasm / Alzheimer's Disease, Type II
Dystonia, Blepharospasm / Meige Syndrome
Dystonia, Blepharospasm / Tardive Dyskinesia
Dystonia, DYT1 GAG Deletion
Dystonia, Focal / Meige Syndrome
Dystonia, Generalized, Adult Onset, Progressive
Dystonia, Generalized, Childhood Onset
Dystonia, Generalized, Familial
Dystonia, Generalized, Familial / Meige Syndrome
Dystonia, Medication Induced
Dystonia, Medication Induced / Schizophrenia
Dystonia, Spasmodic Torticollis
Dystonia, Suspected
Dystonia, Unaffected Relative
Encephalitis (Japanese B)
Encephalocele
Encephalopathy, Demyelinating
Encephalopathy, Unknown Etiology
Encephalomyopathy, X-Linked
Ependymoma
Epidermolysis Bullosa
Extreme Immaturity
Facioscapulohumeral Muscular Dystrophy
Facioscapulohumeral Muscular Dystrophy*
Failure to Thrive, Severe
Fragile X
Fragile X, Carrier
Fragile X, Carrier / Parkinson's Disease
Friedreich's Ataxia
Friedreich's Ataxia, SCA7
Fryns Syndrome
Gaucher Disease
Glioblastoma Multiforme (WHO grade IV)
Glioblastoma Multiforme (WHO grade IV) / Schizophrenia
Glycogen Storage Disease, NOS
Glycogenosis, Type IX
Hallerman Strieff Syndrome
Hemochromatosis, Neonatal
Hippocampal Sclerosis
Hirschsprung's Disease
Holoprosencephaly
Holoprosencephaly / Developmental Delay
Holoprosencephaly / Roberts Sc Syndrome
Homocystinuria
Hunter's Syndrome
Huntington's Disease
Huntington's Disease, Suspected
Hydranencephaly
Hydrocephalus
Hydrocephalus / Mental Retardation
Hydrocephalus, Etiology Undetermined
Hydrops Fetalis
Hyperglycemia, Non-ketotic
Hyperplasia, Right Ventricle
Hyperplasia, Maternal
Hyperplasia, Maternal / Prematurity
Ichthyosis / Leukodystrophy, possible
Inclusion Body Myositis
Infarcs, Cystic
Intestinal Lymphangectasia (Opiz BBB Syndrome)
Intracerebral Hematoma / Histiocytosis
Intrauterine Fetal Demise
Intraventricular Hemorrhage
Joseph's Disease
Kawasaki's Disease
Krabbe's Disease
Lactic Acidosis
Lawrence Moon Bardet Biedle Syndrome
Leigh's Disease
Lennox-Gastaut Syndrome
Leukodystrophy
Leukodystrophy, Consistent with MLD
Leukodystrophy, Metachromatic
Leukodystrophy, NFS
Leukodystrophy, Orthochromic, Pigmentary type
Leukodystrophy, Radiation Induced
Leukodystrophy, Sudanophilic
Leukoencephalitis, NOS
Leukoencephalopathy
Lewy Body Dementia
Lissencephaly
Long Chain Fatty Acid Deficiency
Lowe's Syndrome
Lung Transplants, Bilateral
Macrocephaly
Malformation of the Brainstem and Cerebellum
Malignant Hyperthermia
Manic Depression
Maternal Cocaine Abuse
Meckle-Gruber Syndrome
Meningioma*
Mental Retardation, NOS
Mental Retardation, X-Linked
Mental Retardation / Developmental Delay
Metabolic Disorder
Metabolic Disorder (complex)
Metabolic Disorder, Acute (unknown etiology)
Metabolic Disorder, NFS
Metabolic Disorder, Unknown
Metabolic Encephalopathy
Metabolic Encephalopathy with Intractable Seizures
Metabolic Storage Disease
Microcephaly
Microencephaly
Microencephaly / Primary Immuno-deficiency
Microgyria focal
Micropolygria, Heterotopias / Periventricular Leukomalacia
Mitochondrial Disorder
Mitochondrial Disorder, mtDNA Depletion Syndrome*
Motor Neuron Disease, NOS
Movement Disorder, Unknown
Moya Moya Disease / Ammon's Horn Sclerosis
Mucopolysaccharidosis
Mucopolysaccharidosis, Hurler's Syndrome
Mucopolysaccharidosis, Sanfilippo Syndrome
Multiple Anomalies
Multiple Sclerosis
Multiple Sclerosis*
Multiple Sclerosis / Alzheimer's Disease
Multiple Systems Atrophy
Multiple Vascular Malformations
Muscular Dystrophy
Muscular Dystrophy / Diabetes
Muscular Dystrophy, Becker's Type
Muscular Dystrophy, Duchenne
Myasthenia Gravis
Myelomeningocele
Myofibromatosis, Infantile
Myopathy, NFS*
Myotonic Dystrophy
NBIA
Neural Tube Defect
Neuraxonal Dystrophy
Neurodegenerative Disorder, NOS
Neurodegenerative Disorder, suggestive of Parkinson
Neurofibromatosis
Neurofibromatosis*
Neurofibromatosis, Type I
Neurofibromatosis, Type I and Glioblastoma
Neurofibromatosis, Type I*
Neurofibromatosis, Type II
Neurofibromatosis, Type Unknown
Neuromuscular Disorder Undiagnosed
Neuronal Ceroid Lipofuscinosis
Niemann-Pick Disease, Type C
Nonketotic Hyperglycinemia
Noonan's Syndrome
Noonan's Syndrome*
Obesity
Ogilvies Syndrome
Ohtahara's Syndrome
Oligohydramnios
Olivopontocerebellar Degeneration
Orbital Encephalocele
Ornithine Transcarbamylase Deficiency
Osler Weber Rendau Syndrome
Osteogenesis Imperfecta
Osteomyelitis
Othara Syndrome / Infantile Spasms
Paget Disease, R/O
Parkinson's Disease
Parkinson's Disease / Adrenoleukodystrophy Carrier
Parkinson's Disease / Diabetes
Parkinson's Disease / Multi-Infarct Dementia
Pelizaius-Merzbacher Disorder
Pentalogy of Cantell
Perinatal Asphyxia
Periorbital Hemangioma*
Peripheral Neuropathy, Probable
Peroxisomal Disorder
Phenylketonuria
Polycystic Kidney Disease
Polyhydramnios / Twin to Twin Transfusion Syndrome
Polymicrogryia / Hydrocephalus
Polymyositis / Dermatomyositis
Pompe Disease
Porencephaly
Porencephaly / Systemic Lupus Erythematosus
Posterior Urethral Valve Obstruction
Potter's Syndrome
Prader-Willi Syndrome
Prader-Willi Syndrome*
Prematurity
Progressive Supranuclear Palsy
Propionic Acidemia
Prune Belly Syndrome
Pyruvate Carboxylase Deficiency
Pyruvate Dehydrogenase Deficiency
Renal Agenesis
Renal Osteodystrophy
Retino Blastoma
Retroplacental Hematoma
Rett Syndrome
Rett Syndrome, Uncharacterized Sibling
Sandhoff Disease
Sandhoff Disease*
Sanfilippo Syndrome, Type A
Sanfilippo Syndrome, Type III
Sanfilippo Syndrome, Type III*
Sarcoidosis, Pulmonary
Schizencephaly
Schizo-Affective Disorder
Schizophrenia
Scoliosis
Seizure Disorder
Seizure Disorder*
Seizure Disorder, Post-traumatic
Seizure Disorder, Severe Myoclonic
Seizure Disorder / Blindness
Seizure Disorder / Developmental Disorder
Seizure Disorder / Parkinson's Disease
Severe Movement Disorder
Short Chain Acyl CoA Deficiency
Shy-Drager Syndrome
Sickle Cell Disease
Sirenomelia
Skeletal Dysplasia
Smith-Lemli-Opitz Syndrome
Spina Bifida
Spina Bifida, Arnold-Chiari Malformation II
Spinal Muscular Atrophy
Spinocerebellar Ataxia, Type I
Spinocerebellar Degeneration, Type VII
Status Marmoratus
Stickler Syndrome
Sturge-Weber Syndrome
Sturge-Weber Syndrome*
Sturge-Weber Syndrome, Suspected
Sturge-Weber Syndrome / Alzheimer's Disease
Sturge-Weber Syndrome* / Autism, Suspected*
Sudden Infant Death Syndrome
Sudden Unexplained Death
Suicide
Tar's Syndrome
Tay-Sachs Disease
Tay-Sachs Disease, Suspected
Teratoma
Thanatophoric Dwarfism
Tourettes Syndrome
Toxic/Metabolic (i.e. drug related)
Tracheal Atresia
Trauma, Spinal Cord
Traumatic Brain Injury
Tuberous Sclerosis
Tuberous Sclerosis* / Choroid Plexus Papilloma*
Tuberous Sclerosis*
Tuberous Sclerosis* / Epilepsy*
Undiagnosed Neurological Disorder
Vanishing White Matter Disease
von Hippel-Lindau Disease
von Hippel-Lindau Disease*
von Hippel-Lindau Disease, Suspected*
Walker-Warburg Syndrome
Williams Syndrome
Wolf Parkinson White Syndrome
Zellweger Syndrome
Zellweger's Syndrome, Pseudo
Zellweger, Related, Neonatal ALD