Encephalocraniocutaneous lipomatosis (ECCL) is a rare condition that primarily affects the brain, eyes, and skin of the head and face. Most of this condition's signs and symptoms are present …

Encephalocraniocutaneous lipomatosis (ECCL), is a rare condition primarily affecting the brain, eyes, and skin of the head and face. [2] It is characterized by unilateral subcutaneous and …

Encephalocraniocutaneous lipomatosis is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, …

Dec 1, 2024 · Encephalocraniocutaneous lipomatosis (ECCL), also known as Haberland syndrome, is a sporadic tumor predisposition neurocutaneous disorder, included in the …

Apr 4, 2016 · Encephalocraniocutaneous lipomatosis (ECCL) is a neurocutaneous disorder characterized by ocular anomalies, skin lesions, and central nervous system (CNS) anomalies …

Jun 1, 2022 · Encephalocraniocutaneous lipomatosis (ECCL) is a rare, congenital, neurocutaneous disorder with unilateral lipomatous cutaneous neoplasms devoid of hair and …

Jan 13, 2024 · Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital syndrome with complex skin, eye, and central nervous system (CNS) symptoms. Diagnosis and treatment are …

Encephalocraniocutaneous lipomatosis (ECCL) is a rare, sporadic neurocutaneous disorder present from birth that primarily affects the skin, eyes, and central nervous system of the head …

Background: Encephalocraniocutaneous lipomatosis (ECCL) is a sporadically occurring neurocutaneous disorder of unknown aetiology. It has repeatedly been discussed as a …

Jan 27, 2022 · Encephalocraniocutaneous lipomatosis (ECCL) comprises a spectrum of predominantly congenital anomalies.