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Possible Causes For Microcephaly/oligophrenia - Causes

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Microcephaly/oligophrenia - Causes
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Electromagnetic, Physics, trauma, Radiation Causes: Encephalopathy/postanoxic
Infectious Disorders (Specific Agent): Newborn TORCH syndrome; Cytomegalic virus, congenital; Rubella, congenital; Toxoplasmosis, congental
Infected organ, Abscesses: Neonatal meningitis
Metabolic, Storage Disorders: HyperArgininemia; Phenylketonuria/PKU; Ceroid lipofuschinosis/Late infantile (Jansky); Infantile ceroid lipofuscinosis/Finnish (Santvuori-Haltia)
Deficiency Disorders: Malnutrition, fetal; Malnutrition/Starvation; Marasmus/inanition/cachexia infant; Newborn Low Birth Weight
Congenital, Developmental Disorders: Down's Syndrome; CHARGE Congenital syndrome; Cretinism, goitrous sporadic; Infantile muscle spasms/Hypsarrhythmia; Placenta insufficiency syndrome/infant; Cretinism; Cri du Chat/Chromosome 5p (5p15.2); Microcephaly/oligophrenia; Neonatal Graves/thyrotoxicosis disease; Trisomy-21 partial translocation; Allan-Herndon Mental Retardation/X-linked; Aicardi syndrome; Happy puppet syndrome/Angelman syndrome; Anencephaly/congenital syndrome; Chromosome 4p-syndrome; Chromosome, long-arm 18 deletion synd; De Lange syndrome; Dubowitz syndrome; Hallermann-Streiff-Francois syndrome; Laron dwarfism/GH receptor defect; Renpennings's syndrome; Rett's syndrome; Rubinstein-Taybi syndrome; Trisomy 13 syndrome; Trisomy-18 syndrome; Velocardiofacial (22q gene) syndrome; 13q chromosome deletion; Acro-Facial dysostosis/Nager type; Birth asphyxia Syndrome/Hypoxic event; Cohen Syndrome; Fetal CVA disorder; Thyroid hormone resistance/receptor defect (3p24.3); Trisomy 12 syndrome
Hereditary, Familial, Genetic Disorders: Xeroderma/Dry skin; Juberg Marsidi Genetic syndrome (unco); Beckwith-Wiedemann Syndrome; Alpers cerebral degeneration of infancy; Bird-headed dwarf of Seckel; Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3); Cockayne syndrome; Fanconi's pancytopenia-dysmelia synd; Incontinentia pigmenti/hereditary; Meckel-Gruber syndrome; Menkes steely hair disease; Pelizaeus-Merzbacher disease; Sjogren-Larsson syndrome; Smith-Lemli-Opitz syndrome; 18p chromosome deletion complex; Abducted thumbs syndrome; Andermann Syndrome; Cerebrocostomandibular CCM Syndrome; Chromosome 20 deletion/Ring syndrome; Chudley Syndrome 1; Kabuki make-up syndrome; Lissencephaly/Norman Roberts (7q22)Miller-Dieker (17p13.3); Michelin tire baby syndrome; Neu Laxova Syndrome; Orocraniodigital (Juberg-Hayward) Syndrome; Say Syndrome 1
Vegetative, Autonomic, Endocrine Disorders: Hypothyroidism (myxedema); Pituitary hypothyroidism; Primary hypothyroidism/myxedema; Dwarfism, panhypopituitary; Growth hormone deficiency; Hypothyroidism, juvenile; Panhypopituitarism
Pathophysiologic: Fetal hypoxia/anoxia
Drugs: Warfarin embryopathy syndrome; Fetal Hydantoin Syndrome
Poisoning (Specific Agent): Mercury/organic/methyl (Minamata) pois.; Fetal alcohol syndrome
Organ Poisoning (Intoxication): Drug Induced Fetal Anomalies; Maternal Teratogen Exposure
Synonyms: OLIGOPHRENIA
Definition: Be the first to add a definition for Microcephaly/oligophrenia - Causes
External Links Related to Microcephaly/oligophrenia - Causes: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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