The Experts below are selected from a list of 2214 Experts worldwide ranked by ideXlab platform
Ligia Brzezińska-wcisło - One of the best experts on this subject based on the ideXlab platform.
-
"Scleroderma linearis: hemiatrophia faciei progressiva (Parry-Romberg syndrom) without any changes in CNS and linear Scleroderma "en coup de sabre" with CNS tumor
BMC Neurology, 2009Co-Authors: Beata Bergler-czop, Anna Lis-Święty, Ligia Brzezińska-wcisłoAbstract:Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with Limited Scleroderma linearis. Linear Scleroderma "en coup de sabre" is characterized by clinical presence of most commonly one-sided linear syndrome. In a number of patients, neurological affection is the medium of the disease. The treatment of both Scleroderma varieties is similar to the treatment of Limited systemic sclerosis. Case presentation We present two cases of a disease: a case of a 49-year-old woman with a typical image of hemifacial atrophy, without any changes of the nervous system and a case of a 33-year-old patient with an "en coup de sabre" Scleroderma and with CNS tumor. Conclusion We described typical cases of a rare diseases, hemifacial atrophy and "en coup de sabre" Scleroderma. In the patient diagnosed with Parry-Romberg syndrome, with Borrelia burgdoferi infection and with minor neurological symptoms, despite a four-year case history, there was a lack of proper diagnosis and treatment. In the second patient only skin changes without any neurological symptoms could be observed and only a precise neurological diagnosis revealed the presence of CNS tumor.
Ligia Brzezinskawcislo - One of the best experts on this subject based on the ideXlab platform.
-
Scleroderma linearis hemiatrophia faciei progressiva parry romberg syndrom without any changes in cns and linear Scleroderma en coup de sabre with cns tumor
BMC Neurology, 2009Co-Authors: Beata Berglerczop, Anna Lisświety, Ligia BrzezinskawcisloAbstract:Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with Limited Scleroderma linearis. Linear Scleroderma "en coup de sabre" is characterized by clinical presence of most commonly one-sided linear syndrome. In a number of patients, neurological affection is the medium of the disease. The treatment of both Scleroderma varieties is similar to the treatment of Limited systemic sclerosis.
Beata Bergler-czop - One of the best experts on this subject based on the ideXlab platform.
-
"Scleroderma linearis: hemiatrophia faciei progressiva (Parry-Romberg syndrom) without any changes in CNS and linear Scleroderma "en coup de sabre" with CNS tumor
BMC Neurology, 2009Co-Authors: Beata Bergler-czop, Anna Lis-Święty, Ligia Brzezińska-wcisłoAbstract:Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with Limited Scleroderma linearis. Linear Scleroderma "en coup de sabre" is characterized by clinical presence of most commonly one-sided linear syndrome. In a number of patients, neurological affection is the medium of the disease. The treatment of both Scleroderma varieties is similar to the treatment of Limited systemic sclerosis. Case presentation We present two cases of a disease: a case of a 49-year-old woman with a typical image of hemifacial atrophy, without any changes of the nervous system and a case of a 33-year-old patient with an "en coup de sabre" Scleroderma and with CNS tumor. Conclusion We described typical cases of a rare diseases, hemifacial atrophy and "en coup de sabre" Scleroderma. In the patient diagnosed with Parry-Romberg syndrome, with Borrelia burgdoferi infection and with minor neurological symptoms, despite a four-year case history, there was a lack of proper diagnosis and treatment. In the second patient only skin changes without any neurological symptoms could be observed and only a precise neurological diagnosis revealed the presence of CNS tumor.
Beata Berglerczop - One of the best experts on this subject based on the ideXlab platform.
-
Scleroderma linearis hemiatrophia faciei progressiva parry romberg syndrom without any changes in cns and linear Scleroderma en coup de sabre with cns tumor
BMC Neurology, 2009Co-Authors: Beata Berglerczop, Anna Lisświety, Ligia BrzezinskawcisloAbstract:Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with Limited Scleroderma linearis. Linear Scleroderma "en coup de sabre" is characterized by clinical presence of most commonly one-sided linear syndrome. In a number of patients, neurological affection is the medium of the disease. The treatment of both Scleroderma varieties is similar to the treatment of Limited systemic sclerosis.
Anna Lis-Święty - One of the best experts on this subject based on the ideXlab platform.
-
"Scleroderma linearis: hemiatrophia faciei progressiva (Parry-Romberg syndrom) without any changes in CNS and linear Scleroderma "en coup de sabre" with CNS tumor
BMC Neurology, 2009Co-Authors: Beata Bergler-czop, Anna Lis-Święty, Ligia Brzezińska-wcisłoAbstract:Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with Limited Scleroderma linearis. Linear Scleroderma "en coup de sabre" is characterized by clinical presence of most commonly one-sided linear syndrome. In a number of patients, neurological affection is the medium of the disease. The treatment of both Scleroderma varieties is similar to the treatment of Limited systemic sclerosis. Case presentation We present two cases of a disease: a case of a 49-year-old woman with a typical image of hemifacial atrophy, without any changes of the nervous system and a case of a 33-year-old patient with an "en coup de sabre" Scleroderma and with CNS tumor. Conclusion We described typical cases of a rare diseases, hemifacial atrophy and "en coup de sabre" Scleroderma. In the patient diagnosed with Parry-Romberg syndrome, with Borrelia burgdoferi infection and with minor neurological symptoms, despite a four-year case history, there was a lack of proper diagnosis and treatment. In the second patient only skin changes without any neurological symptoms could be observed and only a precise neurological diagnosis revealed the presence of CNS tumor.