Disease Information for De Lange syndrome
Amstelodamensis Typus Degenerativus, Amsterdam dwarf, Amsterdam type, BDLS, Brachmann Cornelia de Lange (BCDL) syndrome (BDLS), Brachmann Cornelia de Lange syndrome, Brachmann de Lange syndrome, Bruck de Lange, Bruck de Lange syndrome, CDL, CDLS, CDLS1, Cornelia de Lange (CDL) syndrome (CLS) 1, Cornelia de Lange 1, Cornelia de Lange syndrome, CORNELIA DE LANGE SYNDROME 1, Cornelia de Lange's syndrome, De Lange, de Lange syndrome, De Lange syndrome (disorder), de Lange syndrome 1, DE LANGES SYNDROME, De Lange's syndrome, Degener amsterodamensis typus, Degenerative amstelodamensis typus, Degenerative amsterodamensis typus, Dwarf Amsterdam, Lange syndrome 1 Amsterdam dwarf, status degenerativus amstelodamensis, Syndrome Brachmann De Lange, Syndrome De Lange, Syndrome De Lange's, typus amstelodamensis, Typus Degenerativus Amstelodamensis
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Amstelodamensis Typus Degenerativus, Amsterdam dwarf, Amsterdam type, BDLS,... (more)
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-Cornelia de Lange syndrome; de Lange’s syndrome
This condition is described sometimes as one syndrome, sometimes as two; It is here entered as one entity;
A rare form of oligophrenia comprising microcephaly with severe mental retardation, short stature, and characteristic facies; Craniofacial features consist of a clown-like appearance with large, low and curly eyelashes, micrognathia, thin lips and downturned upper lip (carp mouth), cleft lip and palate, optic atrophy, an upturned nose, and hirsutism; The most striking feature of the syndrome is that all the children look alike, like brothers and sisters; Often severe dysplasia of extremities; There is a lobster-claw deformity of the hand, small hands and feet with small and tapered digits, syndactyly between the second and third toes, proximal insertion of the thumb, short and curved fifth finger, phocomelia, and oligodactyly; various other malformations; Cutis marmorata, circumoral cyanosis, generalized hypertrichosis, hypoplastic nipples and umbilicus, and simian creases are the principal dermatological features; Low birth weight after full-term pregnancy and a low-pitched growling cry are the early symptoms; The majority of those affected have diminished sucking and swallowing capacity, failure to thrive, predisposition to respiratory tract infections, and frequent vomiting with aspiration pneumonia; Mental retardation is usually severe; Most patients die before the age of 6 years --------------[whonamedit.com 2005]------------------
Several types described, more severe from duplication of the long arm of chromosome 3
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A syndrome characterized by growth retardation, severe MENTAL RETARDATION, ... (more) (edit)
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Demographics & Risk Factors[next]
- Population Group
- Population/Pediatrics population
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Population Group
Clinical Manifestations[previous][top][next]
- Typical Clinical Presentation
- Presentation/Multiple deformities newborn (odd look)
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Signs & Symptoms
- Child
- Congenital low hairline
- Particular physiognomy/Odd looking kids
- Anteverted Nares deformity
- Craniofacial Abnormalities/Congenital
- Depressed nasal bridge
- Downturned corners of mouth/Carp mouth
- Facies particular
- Hairy forehead
- Long Philtrum/Facies
- Small nipples
- Congenital bushy eyebrows/long lashes/low hair line
- Dermatoglyphic anomalies
- Hair line low
- Hirsutism
- Palm/simian crease (single)
- Poor weight gain/child
- Small umbilicus
- Bifid uvula
- Fish-shaped mouth deformity
- High arched palate
- Increased spacing between teeth/sign
- Receding chin deformity
- Hypotonia
- Claw hand deformity/sign
- Odd body posturing
- Psychomotor retardation
- Abnormal Head Shape/Child
- Bowing of extremities
- Enlarged/deformed joints
- Low set/odd position thumbs
- Missing digits/Oligodactyly
- Proximal placed thumbs deformity
- Low pitched/growling cry
- Nose short/upturned
- Small nose
- Short stature
- Short stature/child
- Eyebrows join in center/Synophrys
- Long eyelashes
- Low set ears/congenital
- Typical Clinical Presentation
Associated Diseases & Rule outs[previous][top][next]
- Associated Disease & Complications
- Atrial septal defect
- Brachycephaly
- Cleft lip/deformity
- Cleft palate/deformity
- Congenital diaphragmatic hernia
- Congenital urinary tract malformations
- Craniosynostosis
- Cryptorchidism
- Cutis marmorata
- Cutis marmorata/newborn
- De Lange Syndrome/Cornelia de Lange
- Dwarfism
- Esophageal stricture/stenosis
- Growth retardation/failure
- Hypertelorism/Wide Spaced Eyes
- Hypospadius anomaly
- Intestine malrotation
- Kidney agenesis/dysplasia unilateral
- Limb deformities/anomalies
- Lobster claw deformity/split hand syndrome
- Malrotation/colon, congenital
- Meckel diverticulum
- Mental retardation
- Microcephaly/oligophrenia
- Micrognathia/congenital small chin
- Multiple congenital anomalies
- Multiple congenital anomalies/Mental retardation
- Patent ductus arteriosis
- Phocomelia
- Syndactyly/Webbing
- Torticollis, congenital
- Ventricular septal defect
- Hand anomalies
- Associated Disease & Complications
Disease Mechanism & Classification[previous][top][next]
- Class
- CLASS/Jablonski/NIH Archive Anomalies Database
- CLASS/Pediatric disorders (ex)
- CLASS/Systemic/no comment (category)
- Pathophysiology
- Pathophysiology/Gene locus chromosome 3
- Pathophysiology/Gene Locus chromosome 3q
- Pathophysiology/Sporadic/hereditary/process
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Congenital/developmental (category)
- PROCESS/Eponymic (category)
- PROCESS/Genetic disorder/Spontaneous mutations/sporadic
- PROCESS/Hereditary dominance/incomplete penetrance (ex).
- PROCESS/Hereditary Multiple anomalies syndrome [EX]
- PROCESS/Hereditofamilial (category)
- PROCESS/INCIDENCE/Rare disease (ex)
- PROCESS/Multiple dysmorphic syndrome (ex)
- PROCESS/Dystostosis/craniofacial (ex)
- Class
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- Synonym
- Synonym/Amsterdam dwarf syndrome of De Lange
- Synonym/Brachmann-Cornelia de Lange syndrome
- Synonym/Cornelia De Lange syndrome
- Synonym/de Lange syndrome I
- Synonym/Status degenerativus amstelodamensis (de Lange)
- Synonym
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