Erschienen in:
26.03.2023 | CASE REPORT
Haberland Syndrome Associated with Juvenile Ossifying Fibroma and Odontoma: Rare Case Report
verfasst von:
Ragavi Alagarsamy, Ongkila Bhutia, Ajoy Roychoudhury, Babu Lal, Rahul Yadav, Deepika Mishra
Erschienen in:
Journal of Maxillofacial and Oral Surgery
|
Ausgabe 1/2024
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Excerpt
Encephalocraniocutaneous lipomatosis (ECCL) also known as Haberland syndrome is a rare neurocutaneous syndrome characterized by involvement of tissues of mesodermal and ectodermal origin such as skin, eyes, adipose tissue, and brain. This rare disorder was first reported in a 5 1/2-year-old epileptic, mentally retarded boy in 1970 by Catherine Haberland and Maurice Perou [
1]. Since then around 70 cases have been reported worldwide as per our knowledge. …