نتایج جستجو برای: cutis marmorata telangictatica congenital

تعداد نتایج: 122724  

Journal: :La Pediatria medica e chirurgica : Medical and surgical pediatrics 2014
C De Maio G Pomero A Delogu E Briatore M Bertero P Gancia

Cutis Marmorata Telangiectatica Congenita (CMTC) is a rare, sporadic condition usually present at birth characterized by localized or generalized persistent cutis marmorata, telangiectasia and phlebectasia. We report a preterm female newborn, the third child of non-related caucasian parents, with CMTC at birth who showed typical cutaneous features and monolateral congenital glaucoma. The pathog...

Journal: :Archivos argentinos de pediatria 2016
Ozkan Ilhan Esra A Ozer Senem A Ozdemir Sinem Akbay Seyma Memur Berat Kanar Melek Akar Sumer Sutcuoglu Mustafa M Tatli

Cutis marmorata telangiectatica congenita (CMTC) is a rare, commonly benign, congenital, localized or generalized vascular anomaly of unknown aetiology. It is characterized by persistent cutis marmorata, telangiectasia and phlebectasia. Extracutaneous findings may be associated with CMTC in 18.8-70% of the cases. Diagnosis of the disorder is based on the clinical findings. The prognosis is good...

Journal: :Archives of dermatology 2009
Dakara Rucker Wright Ilona J Frieden Seth J Orlow Helen T Shin Sarah Chamlin Julie V Schaffer Amy S Paller

BACKGROUND The condition known as macrocephaly-cutis marmorata telangiectatica congenita syndrome (M-CMTC) is a rare congenital syndrome of unknown etiology characterized by macrocephaly and vascular lesions that have been described as either cutis marmorata or cutis marmorata telangiectatica congenita (CMTC). Most patients also exhibit facial and limb asymmetry; somatic overgrowth; development...

2018
Uwe Wollina Katlein França Torello Lotti Georgi Tchernev

BACKGROUND Cutis marmorata telangiectatic congenital or Van Lohuizen syndrome is a rare vascular disorder that may be associated with other congenital malformations. Around 300 cases have been reported so far. CASE REPORT We present a 4-year-old girl with Van Lohuizen syndrome of the leg, but without any other malformations. CONCLUSION Neonatal lupus erythematosus may resemble congenital va...

Journal: :Acta neurologica Taiwanica 2008
Tzu-Hui Li Tsung-Hwa Chen Hung-Sheng Lin Chia-Wei Liou Jia-Shou Liu Shun-Sheng Chen Wei-Hsi Chen

PURPOSE Cutis marmorata is a cutaneous livedoid disorder which can be differentiated from livedo reticularis in both clinical and pathological presentations. Unlike Sneddon syndrome, a detailed immunocoagulation profile has not yet been delineated for cutis marmorata in patients with cerebral ischemia. METHODS To analyze the immunocoagulation profile in cutis marmorata patients associated wit...

2015
Han MA Mengsi Liao Shu Qiu Ruijun Luo Rongbiao Lu Chun Lu

Phacomatosis pigmentovascularis is a rare, congenital condition characterized by a combination of cutaneous melanocytic lesions and vascular malformation. We discuss an entirely unique case of Phacomatosis pigmentovascularis with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita, which may represent a heretofore undescribed vari...

2013
Flávia Trevisan Paulo Rowilson Cunha Clóvis Antonio Lopes Pinto Fernanda Gomes Cattete

Neonatal lupus is a rare disease caused by the transplacental transfer of maternal autoantibodies to the foetus, characterized by transient clinical manifestations such as cutaneous, haematological, and hepatobiliary events or permanent such as congenital heart block. The typical cutaneous manifestations include erythematous, scaly, annular or arched lesions on the face, with slight central atr...

2009
Jesus E Dueñas-Arias Eliakym Arámbula-Meraz Luis O Frías-Castro Rosalio Ramos-Payán Jose A Quibrera-Matienzo Fred Luque-Ortega E Maribel Aguilar-Medina

INTRODUCTION Macrocephaly-capillary malformation syndrome is characterized by cutaneous vascular lesions, including cutis marmorata telangiectatica and hemangiomas, associated with congenital anomalies, including macrocephaly, macrosomia, asymmetry and mental retardation. In addition to these cardinal signs, several other clinical conditions have been reported in people with this condition. How...

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