Encephalocraniocutaneous lipomatosis (Haberland syndrome): A rare case report
Haberland syndrome or Fishman syndrome also known as encephalocraniocutaneous lipomatosis (ECCL) is a rare, congenital neurocutaneous disorder. It is characterized by unilateral involvement of skin, eyes and central nervous system. We report the case of a 28-year-old woman who presented with soft li...
Saved in:
Main Authors: | Ashish Jagati (Author), Bela J Shah (Author), Rima Joshi (Author), Trusha Gajjar (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2016-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Encephalocraniocutaneous lipomatosis (Haberland syndrome): A case report and review of literature
by: Kalyan Koti, et al.
Published: (2013) -
Haberland syndrome: Encephalocraniocutaneous syndrome presenting as status epilepticus
by: V S.V. Prasad, et al.
Published: (2020) -
Encephalocraniocutaneous lipomatosis: A rare neurocutaneous syndrome
by: Shipra Agrwal, et al.
Published: (2021) -
Oculoectodermal Syndrome - Encephalocraniocutaneous Lipomatosis Associated with NRAS Mutation
by: Renée J.H. Richters, et al.
Published: (2020) -
A rare case of dysembryoplastic neuroepithelial tumor combined with encephalocraniocutaneous lipomatosis and intractable seizures
by: Jee-Yeon Han, et al.
Published: (2016)