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Microcephaly
Microcephaly
: Genetic-Information
Overview
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Congenital disorders
(15)
Macrocephaly
Holoprosencephaly
Lissencephaly
Congenital disorder
Colpocephaly
Colpocephaly
Anencephaly
Megalencephaly
Acephaly
Currarino syndrome
Cephalic disorder
Seckel syndrome
Congenital rubella syndrome
Cleft palate
Iniencephaly
Porencephaly
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Genetic disorders
(16)
Marfan
Microphthalmia
Chromosome disorders
Galloway Mowat syndrome
Rubinstein-taybi syndrome
Rubinstein-taybi syndrome
Asymmetric crying facies
Cornelia de Lange syndrome
Genetic disorder
Angelman syndrome
Aceruloplasminemia
Acrania
Phenylketonuria
Monosomy
Beckwith wiedemann syndrome
Trisomy 13
Currarino syndrome
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Nervous system
Lissencephaly
Cephalic disorder
Diseases and disorders
(57)
Microcephaly primary autosomal recessive
Syndactyly type i with microcephaly and mental retardation
Mitral valve stenosis
Micrognathia
Mastoiditis
Mastoiditis
Myelofibrosis
Meningococcal meningitis
Growth retardation
Mitral valve prolapse
Meniere
Severe mental retardation
Meralgia paresthetica
Myotubular myopathy
Minimal change disease
Cerebral cysts
Chorioretinitis
Myocarditis
Syndromes
Craniosynostosis
Polymicrogyria, bilateral frontoparietal
Optic atrophy
Galloway syndrome
Hypotonia
Hirschsprung disease
Cytomegalovirus
Neu laxova syndrome
Scleroderma
Hypoparathyroidism
IUGR
Skeletal dysplasia
Pachygyria
Arnold chiari malformation
Dwarfism
Hypoplasia
Microtia
Encephalocele
Male infertility
Hydrocephalus
Macrocephaly
Marfan
Lissencephaly
Microphthalmia
Chromosome disorders
Anencephaly
Asymmetric crying facies
Cornelia de Lange syndrome
Megalencephaly
Currarino syndrome
Angelman syndrome
Aceruloplasminemia
Cephalic disorder
Seckel syndrome
Cleft palate
Phenylketonuria
Porencephaly
Beckwith wiedemann syndrome
Trisomy 13
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Valvular heart disease
Mitral valve replacement
Mitral valve stenosis
Mitral valve prolapse
Symptoms
(10)
Metatarsalgia
Small skull
Facial abnormalities
Delayed development
Severe mental retardation
Severe mental retardation
Intrauterine growth retardation
Short stature
Anencephaly
Hypotonia
Developmental delay
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Common Causes
Congenital CMV
Cri du chat
Down syndrome
Edwards syndrome
Methylmercury poisoning
Toxoplasmosis
Rubinstein-Taybi syndrome
See also
(20)
Morphea
ASPM (Gene)
Homo floresiensis
Myomectomy
Intrauterine growth retardation
Intrauterine growth retardation
Autosomal recessive
Genetic counselling
Short stature
Malabsorption
Brain size
Lateral ventricles
MCPH1
Dysmorphism
Nasal bridge
Head circumference
Malnutrition
Well-baby examination
Peter Morwood
Am. J. Med. Genet.
Fontanelles
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