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Adams Oliver Syndrome
DefinitionDefinition of Adams Oliver Syndrome Adams–Oliver syndrome (AOS) is a rare congenital disorder characterized by defects of the scalp and cranium (cutis aplasia congenita), transverse defects of the limbs, and mottling of the skin. SymptomsSymptoms of Adams Oliver Syndrome The list of signs and symptoms for Adams-Oliver Syndrome:
CausesCauses of Adams Oliver Syndrome To research the causes of Adams-Oliver Syndrome:
DiagnosisDiagnosis of Adams Oliver Syndrome The diagnosis of AOS is a clinical diagnosis based on the specific features described above. A system of major and minor criteria was proposed. The combination of two major criteria would be sufficient for the diagnosis of AOS, while a combination of one major and one minor feature would be suggestive of AOS. There is currently no genetic testing that can be performed in order to confirm or rule out this condition. TreatmentTreatment of Adams Oliver Syndrome Management of AOS is largely symptomatic and aimed at treating the various congenital anomalies present in the individual. When the scalp and/or cranial bone defects are severe, early surgical intervention with grafting is indicated. PrognosisPrognosis of Adams Oliver Syndrome The overall prognosis is excellent in most cases. However, individuals with more severe scalp and cranial defects may experience complications such as hemorrhage and meningitis, leading to long-term disability. Find Diseases Alphabetically
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