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Cri Du Chat Syndrome
Cri du chat syndrome
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Syndromes
(16)
Cutis hyperelastica
49 xxxxy syndrome
Cushings syndrome
Warkany syndrome 2
Turner syndrome
Turner syndrome
22q11.2 deletion syndrome
Angelman syndrome
Trisomy 13
Trisomy 18
Congenital rubella
Fetofetal transfusion
Triple-x females
47,XYY
Hereditary sensory and autonomic neuropathies
Williams syndrome
Wolf-Hirschhorn syndrome
more...
Rare diseases
48,xxxx
49, XXXXX
Chromosome 5q deletion syndrome
Leukodystrophy, globoid cell
Angelman syndrome
Williams syndrome
Genetic disorders
(35)
Chromosomal abnormalities
Smith-lemli-opitz syndrome
Monosomy
Microcephaly
Trisomy 16
Trisomy 16
Aneuploidy
Hyperostosis, cortical, congenital
1p36 deletion syndrome
Chromosomal deletion
Trisomy
Adrenoleuk- odystrophy
Crouzonode- rmoskeletal syndrome
Trisomy 22
Charcot-Marie-Tooth disease, type 4
Glutaricaciduria
Trisomy 9
Jacobsen syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Cutis hyperelastica
48,xxxx
49 xxxxy syndrome
49, XXXXX
Warkany syndrome 2
Turner syndrome
Chromosome 5q deletion syndrome
22q11.2 deletion syndrome
Angelman syndrome
Trisomy 13
Trisomy 18
Triple-x females
47,XYY
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Williams syndrome
Wolf-Hirschhorn syndrome
more...
Medical condition
(54)
Salaam seizures
Conns Syndrome
Mycobacterial
Corpus callosum agenesis
Chromosome 5p- syndrome
Chromosome 5p- syndrome
Acute myeloblastic leukemia with maturation
Severe mental retardation
Acute megakaryoblastic leukemia
Craniofrontonasal dysplasia
Acute lymphoblastic leukemia
Acute promyelocytic leukemia
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Cutis laxa recessive
Chromosome 9 trisomy
Cystathionine beta-synthase deficiency disease
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
49xxxxy syndrome
Congenital arthromyodysplasia
Floating harbor syndrome
Ehlers-danlos syndrome dermatosparaxis type
Chromosome 5 trisomy 5p
Intervertebral disk displacement
Cutis hyperelastica
48,xxxx
49 xxxxy syndrome
Chromosomal abnormalities
Cushings syndrome
22q11.2 deletion syndrome
Angelman syndrome
Trisomy 13
Trisomy 18
Microcephaly
Fetofetal transfusion
Aneuploidy
Triple-x females
47,XYY
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Charcot-Marie-Tooth disease, type 4
Glutaricaciduria
Trisomy 9
Jacobsen syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
more...
Congenital disorders
Cutis hyperelastica
Corpus callosum agenesis
Genetic disorders
Microcephaly
Congenital rubella
Genetics
(8)
Chromosomes
Mosaicism
Chromosome
Satellite chromosome
Congenital disorders
Congenital disorders
Genetic disorders
47,XYY
Chromosomal deletion
more...
Chromosomes
(54)
Autosome
Centromere
Chromatids
Chromosome 18
Chromosome 22
Chromosome 22
Chromosome 5
Karyotype
Short arm
Translocations
AZF1
Allosome
Chromomere
Chromosomal abnormalities
Chromosomal inversion
Chromosome
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 11 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 3 (human)
Chromosome 4 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome conformation capture
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Lampbrush chromosome
Marker chromosome
Proline-Rich Coiled Coil 1
Ring chromosome
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
X chromosome
Y chromosome
more...
Cytogenetics
(20)
Aneuploidy
Autosome
Chromosomal abnormalities
Chromosome
Colcemid
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Karyotype
Monosomy
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Translocations
Trisomy
Uniparental disomy
X chromosome
more...
Symptoms
Micrognathism
Birth mass
Low-set ears
Single transverse palmar crease
Speech impairment
Severe mental retardation
Microcephaly
Gene
FOXO1
MKL1
RBM15
Delta catenin
See also
(18)
Diseases and disorders
Congenital disorders
Conjugated bilirubin
Abl gene
Sex chromosome
Sex chromosome
IgH
Genes on chromosome 5
ICD-O
Denver Developmental Screening Test
Diastasis recti
Epicanthic fold
Inguinal hernia
Www.fivepminus.org
Telomerase reverse transcriptase
Delayed speech
Chromosome (genetic algorithm)
Maternal age
Thoracic nerves
more...
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