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dc.contributor.authorThalange, Nandu
dc.date.accessioned2023-12-18T07:12:39Z
dc.date.available2023-12-18T07:12:39Z
dc.date.issued2023
dc.identifier.other204-2023.125
dc.identifier.urihttps://repository.mbru.ac.ae/handle/1/1390
dc.description.abstractAbstract: Here, we report the case of a rare and complex disorder, rapid-onset obesity with hypothalamic dysfunction, hypoventilation, autonomic dysregulation, and neuroendocrine tumor (ROHHADNET) syndrome, in a threeyear-old girl with no significant medical history. This is the first such case reported from the UAE. ROHHADNET is a rare disorder of respiratory control and autonomic nervous system regulation with endocrine abnormalities. It typically presents in children older than 18 months with rapid weight gain. This is a challenging diagnosis as there is no clear diagnostic test, and treatment is essentially supportive. This report describes a case of ROHHADNET syndrome in a previously well child who presented with rapid weight gain followed by ophthalmoplegia, dysphagia, electrolyte disturbance, and other comorbidities. The paper outlines in detail the clinical course, investigations, and management of ROHHADNET syndrome. Cerebrospinal fluid analysis revealed oligoclonal bands, which have been reported in only two other cases of ROHHADNET syndrome. Our goal in reporting this case is to increase awareness of this condition among clinicians to facilitate early diagnosis and timely management.en_US
dc.language.isoenen_US
dc.subjectNeural Crest Tumoren_US
dc.subjectOligoclonal Bandsen_US
dc.subjectAutonomic Dysregulationen_US
dc.subjectHypothalamic Dysfunctionen_US
dc.subjectRohhadneten_US
dc.subjectRapid-Onset Obesityen_US
dc.titleRapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, Autonomic Dysregulation, and Neuroendocrine Tumor (ROHHADNET) Syndrome: A Case Reporten_US
dc.typeArticleen_US


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