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Severe Mental Retardation
Severe mental retardation
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Related in the Kosmos
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Disability
Fragile x syndrome
Angelman syndrome
ARBD
Intellectual impairment
Fetal alcohol effects
Down syndrome
Symptoms
(12)
Coarse facial features
Short stature
Facial abnormalities
Hypotonia
Prominent forehead
Prominent forehead
Skeletal abnormalities
Low set ears
Motormental retardation
Dyspepsia
Decreased muscle tone
Heart defects
Intellectual impairment
more...
Diseases and disorders
(43)
X-linked mental retardation
Microcephaly
Chromosome disorders
Partial trisomy
Phenylketonuria
Phenylketonuria
Pachygyria
Growth retardation
Sanfilippo syndrome
Inborn error of metabolism
Congenital toxoplasmosis
Cretinism
Hunter syndrome
Cri du chat syndrome
Syndromes
Lissencephaly
Neonatal hypothyroidism
Micrognathia
Urea cycle disorders
Mucopolysa- ccharidosis
Coffin-lowry syndrome
Sotos syndrome
Iodine deficiency
Hartnup disease
Hurler syndrome
Microphthalmia
Uniparental disomy
Tuberous sclerosis
Dwarfism
Carpenter syndrome
Macrocephaly
Trisomy 18
Trisomy 13
Digeorge syndrome
Bardet Biedl Syndrome
Hypoplasia
Prognathism
Fragile x syndrome
Hypotonia
Angelman syndrome
Fetal alcohol effects
Dyspepsia
Heart defects
Down syndrome
more...
Congenital disorders
(10)
Genetic disorders
Holoprosencephaly
Malformations
Microcephaly
Cretinism
Cretinism
ARBD
Lissencephaly
Neonatal hypothyroidism
Fetal alcohol effects
Macrocephaly
more...
Cytogenetics
(20)
Karyotype
Monosomy
Tetrasomy
Trisomy
X chromosome
X chromosome
Autosome
Chromosomal translocation
Chromosome
Chromosome disorders
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Partial trisomy
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Uniparental disomy
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Chromosomes
(57)
Chromosome 15
Chromosome 21
Ring chromosome
Short arm
AZF1
AZF1
Allosome
Autosome
Centromere
Chromatid
Chromomere
Chromosomal inversion
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 11 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 18 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 22 (human)
Chromosome 3 (human)
Chromosome 4 (human)
Chromosome 5 (human)
Chromosome 6 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome conformation capture
Chromosome disorders
Chromosome engineering
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Karyotype
Lampbrush chromosome
Marker chromosome
Personalized medicine
Proline-Rich Coiled Coil 1
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
X chromosome
Y chromosome
more...
Mental retardation
(17)
AAMR
ARBD
Children Are Us Foundation
Down syndrome
Feeble-minded
Feeble-minded
Fetal alcohol effects
Fragile x syndrome
Imbecile
Lead poisoning
Lujan-Fryns syndrome
Mental retardation (Traditional terms)
Moron (psychology)
Neonatal hypothyroidism
People with intellectual impairment
Phenylketonuria
Richard O. Stimson
Up Syndrome
more...
Syndromes
(16)
Rett syndrome
Turner syndrome
Fragile x syndrome
Sanfilippo syndrome
Hunter syndrome
Hunter syndrome
Angelman syndrome
Cri du chat syndrome
ARBD
Fetal alcohol effects
Sotos syndrome
Hurler syndrome
Carpenter syndrome
Trisomy 18
Trisomy 13
Digeorge syndrome
Down syndrome
more...
Pediatrics
Developmental milestone
Denver Developmental Screening Test
Fragile x syndrome
Inborn error of metabolism
Neonatal hypothyroidism
Down syndrome
Genetics
Genetic disorder
X linked
Mosaicism
X-linked recessive
Genetic disorders
Chromosomes
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Glycosaminoglycans
(9)
Dermatan sulfate
Heparan sulfate
Mucopolysaccharide
Chondroitin sulfate
Heparin
Heparin
Heparinoid
Hyaluronan
Keratan sulfate
Restylane
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Medicine
Genet. Couns.
Contractures
Dysmorphic
Diseases and disorders
Pachygyria
Short stature
Developmental milestone
Causes, incidence, and risk factors
(28)
Adrenoleuk- odystrophy
Congenital CMV
Congenital rubella syndrome
Diabetes mellitus
Encephalitis
Encephalitis
Galactosemia
Gene
HIV
Head injury
Hypoglycemia
Intracranial hemorrhage
Intrauterine
Listeriosis
Meningitis
Methylmercury poisoning
Prader-Willi syndrome
Reye's syndrome
Fragile X syndrome
Phenylketonuria
Sanfilippo syndrome
Toxoplasmosis
Hunter syndrome
Developmental milestones
Cri du chat
Chromosome
Lead poisoning
Metachromatic leukodystrophy
Tay-Sachs disease
more...
See also
(20)
Am. J. Med. Genet.
Psychomotor retardation
Genetic counseling
Autosomal recessive trait
Retardation factor
Retardation factor
FMR1
MeCP2
Palpebral fissures
Craniofacial
Clin. Genet.
Incidence
Secondary handicap
Williams syndrome
Idursulfase
Phenylalanine
X-linked dominant
Phenylalanine hydroxylase
Allan-Hern- don-Dudley syndrome
Hypertelorism
Adaptive behavior
more...
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