PMID- 22345790
OWN - NLM
STAT- PubMed-not-MEDLINE
DCOM- 20120823
LR  - 20211021
IS  - 1998-3611 (Electronic)
IS  - 0019-5154 (Print)
IS  - 0019-5154 (Linking)
VI  - 56
IP  - 6
DP  - 2011 Nov
TI  - Overlap of sturge-weber syndrome and klippel-trenaunay syndrome.
PG  - 755-7
LID - 10.4103/0019-5154.91848 [doi]
AB  - Sturge-Weber syndrome is a rare sporadic condition of mesodermal phakomatosis, 
      characterized by purple-colored flat cutaneous cranial (face) hemangiomas (most 
      commonly along the trigeminal nerve), glaucoma and vascular lesions in the 
      ipsilateral brain and meninges. Klippel-Trenaunay syndrome is also an uncommon 
      mesodermal phakomatosis characterized by a triad of cutaneous and visceral 
      hemangiomas, venous varicosities and soft tissue or bone hypertrophy. 
      Sturge-Weber syndrome in combination with Klippel-Trenaunay syndrome is unusual. 
      Because of the rarity, we report here a 3-year-old boy who presented with 
      overlapping features of both the syndromes.
FAU - Purkait, Radheshyam
AU  - Purkait R
AD  - Department of Pediatric Medicine, NRS Medical College and Hospital, Kolkata, 
      India .
FAU - Samanta, Tryambak
AU  - Samanta T
FAU - Sinhamahapatra, Tapankumar
AU  - Sinhamahapatra T
FAU - Chatterjee, Mridula
AU  - Chatterjee M
LA  - eng
PT  - Journal Article
PL  - India
TA  - Indian J Dermatol
JT  - Indian journal of dermatology
JID - 0370750
PMC - PMC3276916
OTO - NOTNLM
OT  - Hemangioma
OT  - Klippel-Trenaunay syndrome
OT  - Nevus flammeus
OT  - Sturge-Weber syndrome
COIS- Conflict of Interest: Nil.
EDAT- 2012/02/22 06:00
MHDA- 2012/02/22 06:01
PMCR- 2011/11/01
CRDT- 2012/02/21 06:00
PHST- 2012/02/21 06:00 [entrez]
PHST- 2012/02/22 06:00 [pubmed]
PHST- 2012/02/22 06:01 [medline]
PHST- 2011/11/01 00:00 [pmc-release]
AID - IJD-56-755 [pii]
AID - 10.4103/0019-5154.91848 [doi]
PST - ppublish
SO  - Indian J Dermatol. 2011 Nov;56(6):755-7. doi: 10.4103/0019-5154.91848.