phakomatoses

(redirected from Neurocutaneous syndromes)

phakomatoses

phakos, Greek, lens Neurocutaneous syndromes A group of inherited conditions–many are AD–that cause disordered growth of ectodermal tissues, with distinctive skin lesions and tumors and/or defects of the nervous system and/or retina
Phakomatoses
Ataxia-telangiectasia An AR disorder characterized by cerebellar ataxia, oculomotor apraxia, telangiectasias of bulbar conjunctiva, skin of ears, and skin folds–appearing by age 3–and sinopulmonary infections; telangiectasias later extend to the butterfly region of the face; most Pts die in adolescence
Basal cell nevus syndrome See there.
Nevus sebaceous of Jadassohn An occasionally AD clinical condition characterized by a congenital solitary lesion most often present in the scalp which, when large, may be associated with internal derangements eg intracranial masses, seizures, mental retardation, skeletal abnormalities, pigmentary changes, ocular lesions and renal hamartomas; 10% of the skin lesions develop into basal cell carcinoma
Sturge-Weber disease Encephalotrigeminal angiomatosis An occasionally AD condition characterized by congenital capillary hemangiomas of the head & neck, following normal developmental milestones, mental retardation may ensue, caused in part by the sluggish flow of blood through the pial vessels and venous hemangiomas in the leptomeninges and frontoparietal cortex with ipsilateral port-wine nevi, 'tram-track' radiopacities on the skull caused by calcification of the cerebral cortex
Tuberous sclerosis Bourneville-Pringle disease An AD disorder–50% arise de novo Clinical Convulsions, seizures, mental retardation, skin lesions–adenoma sebaceum, sebaceous gland atrophy, angiofibromas, dermal fibrosis with dilated capillaries, shagreen patches, cardiac rhabdomyomas, pulmonary fibrosis, bronchiolar hematomas, bilateral tubular adenomas of kidneys, pancreatic cysts, angiomyolipomas, myxedematous glossitis, spina bifida
von Hippel-Lindau disease An AD condition with retinal hemangioblastoma, ↓ erythropoietin production, cerebellar hemangioblastoma Clinical Ataxia, headache, papilledema, angiomas of the liver, kidney, renal adenomas, papillary cystadenomas of epididymis, pancreatic cysts, adrenal pheochromocytomas;14 develop renal cell cancer
von Recklinghausen disease A relatively common–1/3500 AD condition Clinical Neurofibromas, cafe-au-lait spots of skin, scoliosis, gliosis, glioblastoma multiforme, ependymoma, meningioma and schwannoma, 5-10% sarcomatous degeneration, spina bifida and glaucoma. See Neurofibromatosis.
Note: Neurofibromatosis, tuberous sclerosis, and von Hippel disease constitute the 'classic' phakomatoses

phakomatoses

A group of disorders that involve developmental abnormalities of tissue of ectodermal origin-tissue that gives rise to the skin and the nervous system. The three principal phakomatoses are TUBEROUS SCLEROSIS, VON HIPPEL-LINDAU DISEASE and the STURGE-WEBER SYNDROME.
References in periodicals archive ?
In infancy and childhood, inborn errors of metabolism and developmental disorders such as neuronal migration anomalies and neurocutaneous syndromes predominate as identifiable causes.
Epilepsy in the setting of neurocutaneous syndromes.
In approximately 75% of the patients, seizures are related to cortical malformations, perinatal events, neurocutaneous syndromes (tuberosclerosis, Sturge Weber .
It is appropriate even in the setting of severe developmental delays, widespread areas of abnormality and neurocutaneous syndromes.
FGF23, FRP4, MEPE) by tumour Neurocutaneous syndromes e.
More than 40 neurocutaneous syndromes have been described, the most common of which are neurofibromatosis I and II, tuberous sclerosis, Sturge-Weber syndrome, and von Hippel-Lindau syndrome.
The neurocutaneous syndromes are unique for their neurological and cutaneous manifestations.
Children with neurocutaneous syndromes, who are prone to both benign and malignant tumours.