Diagnostic Challenge of Sturge Weber Syndrome Phenotype in Camp Setting
Author(s) -
Annvi singh,
Rahul Kumar Gupta,
Ashwani Tandon
Publication year - 2022
Publication title -
nmo journal
Language(s) - English
Resource type - Journals
eISSN - 2348-3806
pISSN - 2950-5933
DOI - 10.53772/nmo.2022.16113
Subject(s) - sturge–weber syndrome , phenotype , medicine , dermatology , genetics , biology , gene
Sturge Weber angiomatosisis a non-developmental, rare condition with a vascular hamartomata’s involving the tissues of brain and face. We report herewith a case presenting with recurrent seizures and facial port wine stain in a camp of tribal area in Central India. This patient presentation mimic phenotype of Sturge Weber Syndrome.
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