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 DeCS Categories

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.370 Dysostoses .
C05.116.099.370.894 Synostosis .
C05.116.099.370.894.232 Craniosynostoses .
C05.660 Musculoskeletal Abnormalities .
C05.660.207 Craniofacial Abnormalities .
C05.660.207.240 Craniosynostoses .
C05.660.906 Synostosis .
C05.660.906.364 Craniosynostoses .
C10 Nervous System Diseases .
C10.500 Nervous System Malformations .
C10.500.680 Neural Tube Defects .
C10.500.680.488 Encephalocele .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.621 Musculoskeletal Abnormalities .
C16.131.621.207 Craniofacial Abnormalities .
C16.131.621.207.240 Craniosynostoses .
C16.131.621.906 Synostosis .
C16.131.621.906.364 Craniosynostoses .
C16.131.666 Nervous System Malformations .
C16.131.666.680 Neural Tube Defects .
C16.131.666.680.488 Encephalocele .
C23 Pathological Conditions, Signs and Symptoms .
C23.300 Pathological Conditions, Anatomical .
C23.300.707 Hernia .
C23.300.707.186 Encephalocele .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.210 Contractile Proteins .
D12.776.210.500 Muscle Proteins .
D12.776.210.500.410 Dystrophin-Associated Proteins .
D12.776.210.500.410.500 Dystroglycans .
D12.776.220 Cytoskeletal Proteins .
D12.776.220.362 Dystrophin-Associated Proteins .
D12.776.220.362.249 Dystroglycans .
D12.776.543 Membrane Proteins .
D12.776.543.268 Dystrophin-Associated Proteins .
D12.776.543.268.500 Dystroglycans .
I01 Social Sciences .
I01.076 Anthropology .
I01.076.368 Anthropology, Physical .
I01.076.368.239 Craniology .
 
 Terms
 Synonyms & Historicals		Documents
LILACS e MDL		 
Nervous System Malformations .
Abnormalities, Congenital, Nervous System .
Abnormalities, Nervous System .
Anomalies, Nervous System .
Congenital Abnormalities, Nervous System .
Congenital Anomalies, Nervous System .
Congenital Malformations, Nervous System .
Cranioschisis .
Malformations, Nervous System, Congenital .
Nervous System Anomalies .
Nervous System Congenital Abnormalities .
Nervous System Congenital Malformations .
Nervous System Malformations, Congenital .
Abnormality, Nervous System .
Anomaly, Nervous System .
Cranioschises .
Malformation, Nervous System .
Malformations, Nervous System .
Nervous System Abnormality .
Nervous System Anomaly .
Nervous System Malformation .
Nervous System Abnormalities .
NERVOUS SYSTEM MALFORMATION .
Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis. .
1.00
641744
 
Neural Tube Defects .
Acrania .
Developmental Neural Tube Defects .
Iniencephaly .
Neural Tube Developmental Defects .
Neuroenteric Cyst .
Occult Spinal Dysraphism .
Occult Spinal Dysraphism Sequence .
Tethered Spinal Cord Syndrome .
Acranias .
Craniorachischises .
Cyst, Neurenteric .
Cyst, Neuroenteric .
Cysts, Neurenteric .
Cysts, Neuroenteric .
Defect, Neural Tube .
Defects, Neural Tube .
Diastematomyelias .
Dysraphism, Occult Spinal .
Dysraphisms, Occult Spinal .
Exencephalies .
Iniencephalies .
Myelodysplasia, Spinal Cord .
Myelodysplasias, Spinal Cord .
Neural Tube Defect .
Neurenteric Cysts .
Neuroenteric Cysts .
Occult Spinal Dysraphisms .
Spinal Cord Myelodysplasias .
Spinal Dysraphism, Occult .
Spinal Dysraphisms, Occult .
Tethered Cord Syndromes .
Craniorachischisis .
Developmental Defects, Neural Tube .
Diastematomyelia .
Exencephaly .
Neurenteric Cyst .
Spinal Cord Myelodysplasia .
Tethered Cord Syndrome .
Myelodysplasia .
Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) .
0.78
2497054
 
Craniosynostoses .
Brachycephaly .
Craniostenosis .
Craniosynostosis .
Craniosynostosis, Lambdoidal .
Craniosynostosis, Type 1 .
Lambdoid Synostosis .
Metopic Synostosis .
Plagiocephaly, Craniosynostosis .
Plagiocephaly, Synostotic .
Sagittal Synostosis .
Scaphocephaly .
Synostotic Anterior Plagiocephaly .
Synostotic Posterior Plagiocephaly .
Trigonocephaly .
Unilateral Coronal Synostosis .
1 Craniosynostoses, Type .
1 Craniosynostosis, Type .
Anterior Plagiocephaly, Synostotic .
Coronal Synostoses, Unilateral .
Coronal Synostosis, Unilateral .
Craniostenoses .
Craniosynostose .
Craniosynostoses, Lambdoidal .
Craniosynostoses, Type 1 .
Craniosynostosis Plagiocephaly .
Lambdoid Synostoses .
Lambdoidal Craniosynostoses .
Lambdoidal Craniosynostosis .
Metopic Synostoses .
Plagiocephaly, Synostotic Anterior .
Plagiocephaly, Synostotic Posterior .
Posterior Plagiocephaly, Synostotic .
Sagittal Synostoses .
Synostoses, Lambdoid .
Synostoses, Metopic .
Synostoses, Sagittal .
Synostoses, Unilateral Coronal .
Synostosis, Lambdoid .
Synostosis, Metopic .
Synostosis, Sagittal .
Synostosis, Unilateral Coronal .
Synostotic Plagiocephaly .
Type 1 Craniosynostoses .
Type 1 Craniosynostosis .
Unilateral Coronal Synostoses .
Acrocephaly .
Oxycephaly .
Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS. .
0.65
1283992
 
Dystroglycans .
Cranin .
Dystroglycan 1 .
Dystrophin-Associated Glycoprotein 1 .
alpha-Dystroglycan .
beta-Dystroglycan .
Dystrophin Associated Glycoprotein 1 .
alpha Dystroglycan .
beta Dystroglycan .
Dystroglycan .
Dystrophin-associated proteins that play role in the formation of a transmembrane link between laminin-2 and DYSTROPHIN. Both the alpha and the beta subtypes of dystroglycan originate via POST-TRANSLATIONAL PROTEIN PROCESSING of a single precursor protein. .
0.61
21245
 
Craniology .
The scientific study of variations in size, shape, and proportion of the cranium. .
0.59
5148
 
Encephalocele .
Acquired Encephalocele .
Bifid Cranium .
Cephalocele .
Cerebellar Hernia .
Cerebellar Herniation .
Cranial Meningoencephalocele .
Craniocele .
Cranium Bifidum .
Encephalocele, Acquired .
Encephalocele, Frontal .
Encephalocele, Occipital .
Encephalocele, Sincipital .
Notoencephalocele .
Sincipital Encephalocele .
Tonsillar Hernia .
Tonsillar Herniation .
Acquired Encephaloceles .
Bifid Craniums .
Bifidum, Cranium .
Bifidums, Cranium .
Cephaloceles .
Cerebellar Hernias .
Cerebellar Herniations .
Cerebral Hernia .
Cerebral Hernias .
Cranial Meningoencephaloceles .
Cranioceles .
Cranium Bifidums .
Cranium, Bifid .
Craniums, Bifid .
Encephaloceles .
Encephaloceles, Acquired .
Encephaloceles, Frontal .
Encephaloceles, Occipital .
Encephaloceles, Sincipital .
Frontal Encephaloceles .
Hernia, Cerebellar .
Hernia, Tonsillar .
Hernias, Cerebellar .
Hernias, Cerebral .
Hernias, Tonsillar .
Herniation, Cerebellar .
Herniation, Tonsillar .
Herniations, Cerebellar .
Herniations, Tonsillar .
Meningoencephalocele, Cranial .
Meningoencephaloceles, Cranial .
Notoencephaloceles .
Occipital Encephaloceles .
Sincipital Encephaloceles .
Tonsillar Hernias .
Tonsillar Herniations .
Hernia, Cerebral .
Frontal Encephalocele .
Occipital Encephalocele .
Brain tissue herniation through a congenital or acquired defect in the skull. The majority of congenital encephaloceles occur in the occipital or frontal regions. Clinical features include a protuberant mass that may be pulsatile. The quantity and location of protruding neural tissue determines the type and degree of neurologic deficit. Visual defects, psychomotor developmental delay, and persistent motor deficits frequently occur. .
0.59
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