Disease Information for Down's syndrome
21 trisomy, Chromosomal imbalance syndrome pair 21 trisomy, Chromosome 21 trisomy, chromosome 21 trisomy syndrome, Complete trisomy 21 syndrome, Complete trisomy 21 syndrome (disorder), congenital acromicria syndrome, Down, Down Syndrome, Downs Syndrome, DOWN'S SYNDROME, Down's syndrome trisomy 21, Down's syndrome (disorder), Down's syndrome unspecified, G Trisomy, Langdon Down, Langdon Down syndrome, Mongol, Mongolism, MONGOLOIDISM, morbus Down, Syndrome Down, Syndrome Down's, syndrome trisomy 21, T21 Trisomy 21, Trisomy 21, trisomy 21 syndrome, trisomy syndrome 21
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21 trisomy, Chromosomal imbalance syndrome pair 21 trisomy, Chromosome 21 t... (more)
The most frequently occurring mental retardation/multiple anomaly syndrome usually involving more than 100 individual defects; Typical facies with upslanting palpebral fissures is the characteristic feature of this syndrome (hence the offensive designations "mongoloid idiocy" and "mongolism"); A wide range other defects, such as congenital heart diseases, respiratory disorders, and leukemia, may be associated; Down syndrome patients who survive into late adulthood may develop Alzheimer syndrome----------------------------------------------------------------Down Syndrome; Chromosome 21, Mosaic 21 Syndrome;
Chromosome 21, Translocation 21 Syndrome; Trisomy 21 Syndrome; Trisomy G Syndrome; Down Syndrome is a chromosomal disorder in which all or a portion of chromosome 21 appears three times (trisomy) rather than twice in cells of the body; Symptoms and findings may vary greatly in range and severity, depending on the specific length and location of the duplicated (trisomic) portion of chromosome 21 as well as the percentage of cells containing the abnormality; However, in many affected individuals, such abnormalities may include low muscle tone (hypotonia); a tendency to keep the mouth open with protrusion of the tongue; and distinctive malformations of the head and facial (craniofacial) area, such as a short, small head (microbrachycephaly), upwardly slanting eyelid folds (palpebral fissures), a depressed nasal bridge, a small nose, and a relatively flat facial profile; Individuals with Down Syndrome may also have unusually small, misshapen (dysplastic) ears; a narrow roof of the mouth (palate); vertical skin folds covering the inner corners of the eyes (epicanthal folds); dental abnormalities; and excessive skin on the back of the neck; Abnormalities of the extremities are also often present, such as unusually short arms and legs; short fingers; and unusual skin ridge patterns (dermatoglyphics) on the fingers, palms, and toes; Affected individuals may also have short stature, poor coordination, mild to severe mental retardation, and hearing impairment; In some cases, Down Syndrome may also be characterized by structural malformations of the heart at birth (congenital heart defects); increased susceptibility to respiratory disease ( pneumonia), other infectious diseases, and malignancies including leukemia;
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The most frequently occurring mental retardation/multiple anomaly syndrome ... (more) (edit)
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Demographics & Risk Factors[next]
- Established Disease Population
- Population Group
- Population/Pediatrics population
- Family History
- Sex & Age Groups
- Population/Child
- Population/Children/all
- Population/Infant
Clinical Manifestations[previous][top][next]
- Typical Clinical Presentation
- Presentation/Congestive heart failure/child
- Presentation/Multiple deformities newborn (odd look)
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Signs & Symptoms
- Child
- Infant
- Particular physiognomy/Odd looking kids
- Craniofacial Abnormalities/Congenital
- Facial expression dull/Dull facies
- Facies particular
- Short neck/Brevicollis
- Heart murmur
- Gray Hair
- Grey hair, premature
- Grey hair/childhood
- Palm/simian crease (single)
- Palmar crease variations/aberrancy
- Silvery grey hair/child
- White Hair
- Low birth weight/newborn/SGA/Small for gestational age
- Newborn posterior neck edema/swelling
- Constipation in Children
- Failure to Thrive
- Failure to Thrive Child
- Failure to thrive/infant sign
- Glossoptosis/Swallowing tongue
- Large tongue/macroglossia
- Big toe widely spaced from second (Goldstein) sign
- Central hypotonia, infants
- Hypotonia
- Delayed speech/language development
- Development/motor skills delayed
- Developmental milestones delayed
- Idiocy/signs
- Infant Seizures
- Neonatal hypotonia/floppy-baby sign
- Seizures/Children/recurrent
- Slow Motor Development
- Good bonding social skillsj
- Abnormal Head Shape/Child
- Dysmorphic dwarfism/short stature
- Incurved/fifth fingers
- Delayed speech development/impediment
- Snoring
- Dysmorphic appearance/face
- Neonatal edema/anasarca
- Short stature
- Short stature/child
- Epicanthal folds
- Iris/speckled spots (Brushfield)
- Mongoloid eye slant/congenital/sign
- Anomalous ears/deformities
- Typical Clinical Presentation
Laboratory Tests[previous][top][next]
- Abnormal Lab Findings (Non Measured)
- Abnormal Lab Findings - Decreased
- Abnormal Lab Findings - Increased
Diagnostic Test Results[previous][top][next]
- Other Tests & Procedures
- Pathology
- CT Scan
- X-RAY
Associated Diseases & Rule outs[previous][top][next]
- Associated Disease & Complications
- Acute leukemia
- Alzheimers disease
- Atlanto/axial injury
- Atlanto/odontoid dislocation/fracture
- Atrial septal defect
- Atrioventricular (AV) canal/congenital defect
- Brachycephaly
- Cognitive/learning disability
- Congenital heart disease
- Constipation
- Craniosynostosis
- Cutis marmorata
- Cutis marmorata/newborn
- Dementia
- Down's synrome
- Duodenum, atresia
- Esophagitis
- Esophagitis, reflux/GERD
- Esotropia
- Hirschsprung disease
- Hypermobility joints syndrome
- Hyperthyroidism (Graves disease)
- Hypothyroidism (myxedema)
- Hypouricemia
- Intestinal/bowel obstruction
- Intestine malrotation
- Large bowel obstruction
- Leukemia
- Malrotation/colon, congenital
- Mental retardation
- Microcephaly/oligophrenia
- Obesity
- Obesity in Children
- Obstructive sleep apnea/Children
- Pancytopenia
- Plethora of newborn
- Thyroiditis, Hashimoto's
- Ventricular septal defect
- Childhood Seizures
- Associated Disease & Complications
Disease Mechanism & Classification[previous][top][next]
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Facial area manifestation/disorder (ex)
- CLASS/Systemic/no comment (category)
- Pathophysiology
- Pathophysiology/Chromosomes/47 count
- Pathophysiology/Gene locus 1q43
- Pathophysiology/Gene locus 21q22.3
- Pathophysiology/Gene locus Chromosome 1
- Pathophysiology/Gene locus chromosome 21
- Pathophysiology/Gene locus Chromosome X.
- Pathophysiology/Gene Locus Identified/OMIM database
- Pathophysiology/Gene locus Xp11
- Pathophysiology/Gene locus Xp11.23
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Neurodevelopmental disorders
- Pathophysiology/Extra-chromosomal material present
- Pathophysiology/Aneuploidy (Error Number of Chromosomes)
- Pathophysiology/Chemotaxis failure/phagocytes/effect
- Pathophysiology/Defective leukocyte killing activity
- Process
- PROCESS/Chromosomal disorder (ex)
- PROCESS/Congenital/developmental (category)
- PROCESS/Eponymic (category)
- PROCESS/Genetic mosaicism/possible (ex)
- PROCESS/Hereditofamilial (category)
- PROCESS/Multiple dysmorphic syndrome (ex)
- PROCESS/Pre-Malignant condition (ex)
- PROCESS/Anomalies/Deformities/Malformations (EX)
- PROCESS/Dystostosis/craniofacial (ex)
- Class
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- Synonym
- Synonym/Mongolism
- Synonym/Trisomy-21 syndrome
- Synonym
Treatment[previous][top][next]
- Other Treatments
- TX/Genetic counselling
- Other Treatments
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