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375 Possible Causes for Acquired Microcephaly

  • Malignant Migrating Partial Seizures of Infancy

    microcephaly, and lack of a significant familial and etiological context.[books.google.de] Key features include onset of focal seizures within the first 6 months of life associated with autonomic features, post-natally acquired microcephaly and developmental stagnation[academic.oup.com] […] migrating polymorphous focal seizures, associated with multifocal ictal EEG discharges, progressive deterioration of psychomotor development combined with frequent evolution of acquired[books.google.de]

  • Adrenal Hemorrhage

    microcephaly and blindness.[ncbi.nlm.nih.gov] […] a case of severe perinatal asphyxia with both cerebral venous thrombosis and adrenal hemorrhage who survived with severe sequela including multicystic encephalomalasia, acquired[ncbi.nlm.nih.gov]

  • Xeroderma Pigmentosum Complementation Group B

    Approximately 25% of affected individuals have neurologic manifestations (acquired microcephaly, diminished or absent deep tendon stretch reflexes, progressive sensorineural[ncbi.nlm.nih.gov]

  • Drop Attacks

    Rett syndrome is a neurodevelopmental genetic disorder, characterized by developmental delay, hand stereotypies, abnormal gait, and acquired microcephaly.[ncbi.nlm.nih.gov]

  • Alkalosis

    Aicardi-Goutières syndrome is a rare progressive encephalopathy characterized by acquired microcephaly, basal ganglia calcification, and chronic CSF lymphocytosis, raised[ncbi.nlm.nih.gov]

  • GLUT1 Deficiency Syndrome

    The "classic" GLUT1DS patient presents with infantile seizures (resistant to traditional seizure medications), developmental delay, acquired microcephaly, hypotonia, spasticity[ncbi.nlm.nih.gov] microcephaly, hemolytic anemia, gait disturbance, and dyspraxia in different combinations.[ncbi.nlm.nih.gov] Glucose transporter protein type 1 deficiency syndrome is a metabolic disorder manifesting as cognitive impairment, acquired microcephaly, epilepsy, and/or movement disorder[ncbi.nlm.nih.gov]

  • Xeroderma Pigmentosum

    These include acquired microcephaly, diminished or absent deep tendon stretch reflexes, progressive sensorineural hearing loss, spasticity, ataxia, seizures and progressive[orpha.net] Possible features are hyporeflexia, sensorineural deafness, spasticity, poor co-ordination, seizures, acquired microcephaly or progressive intellectual impairment.[patient.info] microcephaly, decreased or absent deep tendon reflexes, progressive sensorineural deafness, spasticity, ataxia, epilepsy and progressive cognitive impairment).[flipper.diff.org]

  • Macrocephaly

    Microcephaly can present as primary or acquired.[pedsinreview.aappublications.org] Acquired microcephaly is distinguished by a normal head circumference at birth, followed by development of microcephaly in subsequent months or years, usually due to lack[pedsinreview.aappublications.org] Causes of acquired microcephaly include sequelae from stroke, meningitis, or encephalitis; other infections, such as toxoplasmosis, rubella, cytomegalovirus, and herpes; in[pedsinreview.aappublications.org]

  • Brain Atrophy

    Aicardi-Goutières syndrome is a severe and progressive familial encephalopathy that is characterized by acquired microcephaly, intracranial calcification (mainly of the basal[ncbi.nlm.nih.gov]

  • Microcephalic Osteodysplastic Primordial Dwarfism Type II

    Microcephalic osteodysplastic primordial dwarfism type II is a specific disorder characterized by severe intrauterine and postnatal growth retardation, acquired microcephaly[ncbi.nlm.nih.gov] Abstract Microcephalic osteodysplastic primordial dwarfism type II is a specific disorder characterized by severe intrauterine and postnatal growth retardation, acquired microcephaly[unboundmedicine.com] microcephaly, cerebrovascular abnormalities, progressive bone dysplasia, and a characteristic face.[unboundmedicine.com]

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