[Typus degenerativus amstelodamensis. The Cornelia de Lange syndrome in 2 children]. 1979

E Seemanová, and F Losan, and J Salichová

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D008297 Male Males
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D003635 De Lange Syndrome A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231) Brachmann-De Lange Syndrome,Cornelia De Lange Syndrome,CdLS, X-Linked,CdLS2,Cornelia de Lange Syndrome 1,Cornelia de Lange Syndrome 2,Cornelia de Lange Syndrome 3,Cornelia de Lange Syndrome, X-Linked,De Lange's Syndrome,Typus Degenerativus Amstelodamensis,Amstelodamensis, Typus Degenerativus,Brachmann De Lange Syndrome,CdLS, X Linked,CdLSs, X-Linked,Cornelia de Lange Syndrome, X Linked,Syndrome, Brachmann-De Lange,X-Linked CdLS,X-Linked CdLSs
D003878 Dermatoglyphics The study of the patterns of ridges of the skin of the fingers, palms, toes, and soles. Fingerprints,Plantar Prints,Fingerprint,Plantar Print,Print, Plantar,Prints, Plantar
D005149 Facial Expression Observable changes of expression in the face in response to emotional stimuli. Face Expression,Expression, Face,Expression, Facial,Face Expressions,Facial Expressions
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

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