A case of phacomatosis pigmentovascularis with Sturge-Weber syndrome and Klippel-Weber syndrome

1995 ◽  
Vol 17 (6) ◽  
pp. 445-446 ◽  
Author(s):  
Y Arai
2010 ◽  
Vol 27 (3) ◽  
pp. 303-305 ◽  
Author(s):  
Lindsey B. Finklea ◽  
Melinda R. Mohr ◽  
Molly M. Warthan ◽  
David H. Darrow ◽  
Judith V. Williams

2015 ◽  
Vol 30 (4) ◽  
pp. 329-335 ◽  
Author(s):  
Bongjin Lee ◽  
Hyung Joo Jeong ◽  
Yu Hyeon Choi ◽  
Chong Won Choi ◽  
June Dong Park

2021 ◽  
pp. 112067212110678
Author(s):  
Vijaikrishnan Manavalan ◽  
Subashini Kaliaperumal ◽  
Swathi Subramanian ◽  
Malavika Mani

Phacomatosis pigmentovascularis (PPV) is a rare congenital disease characterized by the co-existence of cutaneous vascular malformation and pigmentary nevi with or without extracutaneous systemic involvement. Here, we present a 2-month old child diagnosed with phacomatosis cesioflammea type of PPV with Sturge-Weber syndrome and secondary congenital glaucoma of the left eye. She underwent combined trabeculotomy and trabeculectomy in the left eye for glaucoma and was started on anti-epileptics for seizure control following pediatric evaluation. Early screening and treatment initiation can prevent blindness and other systemic complications associated with PPV.


2000 ◽  
Vol 42 (11) ◽  
pp. 756-759 ◽  
Author(s):  
Uri Kramer ◽  
Esther Kahana ◽  
Zamir Shorer ◽  
Bruria Ben-Zeev

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