Paladini D, et al.: Prenatal diagnosis and hemodynamic evaluation of
Klippel-Trenaunay-Weber syndrome.
Ultrasound Obstet Gynecol. 1998 Sep; 1 2(3):2 15-7.
[MEDLINE record in process]
PMID: 9793196; UI: 99009591.
Palatsi, R.: A Case of the KTPW Syndrome. Acta Derm Venereol,
(Stockholm) 55:3, 1975.
Palier, A.: Vascular Disorders: Review Article: 61 refs. Dermatol Clin.,
5:1, 1987.
Palmer, G., and M. Sheppard: KT Syndrome in Vietnam. Med. J. Aust.,
2:24, 1969.
Parameswara, Y., and R. Naik: KTW Syndrome. Dermatologica1, 64:4,
1982.
Partsch, H.: Clinical Picture of the F.P. Weber Syndrome. Hautarzt,
25:5, 1974.
Patzer-Trazaskowska, T.,I. Skrabalak: KTPW Syndrome with
Simultaneous Consumption Coagulation Disorders in a 14-Year Old
Girl. Pediatr. Pol., 44:5, 1969.
Pawlaczyk, B.,E. Zabel, and K. Dmochowski: A Rare Form of KTW
Syndrome in a 4-month Old Child. Wiad. Lek. 40:2, 1987.
Peixinho, M.,R. Arakaki, and C. Toledo: Correction of Leg Inequality
in the KTW Syndrome. Int. Orthop., 6:1, 1982.
Pellerin, D., H. Martelli, and X. Latouche: Congenital Soft Tissue
Dysplasia: A New Anatomicoclinical entity. Bull. Acad. Natl. Ned. :
Paris, 170:6, 1986.
Perez de la Cruz, J., C. Himenez, and N. Cutillas: Congenital Peripheral
Arteriovenous Fistulas. Rev. Esp. Cardiol., 39:6, 1986.
Phillips, G.,D. Bordon, and E. ,Martin: The KT Syndrome: Clinical and
Radiological Aspects. Radiology, 128:2, 1978.
Pierer, H.: KTW Syndrome from the Surgical Viewpoint. Klin Med
Osterr Z Wiss Prakt Med, 20:6, 1965.
Pilecki, O., and S. Pilecki: Neuroectomesodermal Dysplasia in a Child
with the Clinical Picture of Incomplete KT Syndrome. Wiad Lek, 40:1,
1987.
Pirker, E.: A Roentgenologic Contribution to the Pathogenesis of the
KT Syndrome. Radiol. Austria 5:4, 1966.
Pisko-Dubienski, Z.,R. Baird, and D. Wilson: Identification and
Successful Treatment of Congenital Microfistulas with the Aid of
Directional. DopplerSurgery, 78:5, 1975.
Pitagoras de Mattos, J.: KTPW Syndrome with Spinal Cord Angioma.
Arq Neuropsiquiatr., 33:3, 1975.
Powolny, M.: Pregnancy and Labor in a Woman with KT Syndrome.
Gindkol Pol., 57:3, 1986.
Prigent, F., J. Valleteau de Noulliac, and F. Ramel: KTW Syndrome
with Neonatal Manifestations. Ann Dermatol Venereol1, 10:9, 1983.
Proesmans, W., B. Van Damme and G. Marchal: KT Syndrome with
Systemic Hypertension and Chronic Renal Failure. Ann Pediatr,
(Paris) 29:9, 1982.
Quattrini, A.,P. Bergonzi, and E. Signorini: A Mixed Form of Sturge-
Weber and KT Disease. Riv Neurobiol, 17:3, 1971.
Rabl, C.: Remarkable Orthopedic Findings in a Case of KT disease. Z
Orthop, 1001:1, 1966.
Reynolds, J.,B. Johnson, and S. Gloster: Glaucoma and KTW Syndrome.
Am. J. Ophthalmol,106:4, 1988.
Richards DS, et al.: Sonographic demonstration of widespread uterine
angiomatosis in a pregnant patient with Klippel-Trenaunay-Weber syndrome.
J Ultrasound Med. 1997 Sep; 16(9): 631-3. No abstract available.
PMID: 9321785; UI: 97463001.
Rink T.et al.: [Simultaneous use of different nuclear medical
examinations in Klippel-Trenaunay syndrome--vs.Proteus syndrome].
Nuldearmedizin. 1997 Aug;36(5): 183-6. German.
PMID: 9380531; UI: 97455945.
Ring, D. , and S. Mallory: What Syndrome is This? KT syndrome.
Pediatric Dermatology, 9:1, 1992.
Rivera-Reyes, L., and M. Toro-Sola: Brief Communication: Nevus Unis
Lateris and KTW Syndrome with the Sturge Weber Anomaly in a
Consanguineous Puerto Rican Family. Bol Asoc Med PR, 701:2, 1979.
Robertson, A.: MRI of the Soft Tissues -- Case Reports. Australas
Radiol., 301:3, 1987.
Roebuck DJ. : Klippel-Trenaunay and Parkes-Weber syndromes.
AJR Am J Roentgenol. 1997 Jul;169(1):31 1-2. No abstract available.
PMID: 9207562; UI: 97351280.
Saatci, H.,T. Tuncali, and M. Kroyak: KTW Syndrome with Giant Cysts
in the Lung (author's translation) Prax Pneumol., 30:2, 1976.
Sakai, H.,T. Fuse, and D. Kaneko: Cranial Hemihypertrophy in KT
Syndrome (author's translation) No To Shinkei, 33:5, 1981.
Sanchez, C.,C. Perea, and G. Moreno: Osteohypoplastic Angiomatosis;
Servelle's Syndrome. Med Cutan Ibero Lat Am, 13:3, 1985.
Sarrat, M: KT symdrome. Bord Med, 4:3, 1971.
Sasmaz, O.,S. Devrim, and M. Ozgur: Congenital Arteriovenous Fistulas
of the Extremities: KT syndrome. Tip Fak Mecm, 32:1, 1969.
Schaal, P., and P. Blundell: The KT Syndrome: A Case Report and
Review. J. Cardiovasc. Surg.: Torino, 17:3, 1976.
Schimph, A., and H. Wehberg: Angiokeratoma Maeviforme: Relations
to KTW Syndrome. Z Haut Geschlechtskr, 44:21, 1969.
Schmitt, B., H. Posselt, and K. Waag: Severe Hemorrhage from
Intestinal Hemangiomatosis in KT Syndrome: Pitfalls in Diagnosis and
Management. J. Pediatr. Gastroenterol. Nutr, 5:1, 1986.
Schmutzler, R.: Possibilities of Hemorrhage in the KT Syndrome.
Thromb Diath Haemorrh, 30, 1968.
Schobinger, R.,B. Nachbur, and A. Senn: The Syndrome of KT, A
Polyvalent Angiodysplasia. J. Cardiovasc. Surg. (Torino), 28:5, 1987.
Schofield, D. ,G. Zaatari, and B. Gay: KT and Sturge Weber Syndromes
with Renal Hemangioma and Double Inferior Vena Cava. Journal of
Urology,.136:2, 1986.
Schulz, H., and J. Neumann: Angiodysgenetic Necrotizing Myelopathy
Foix-Alajouanine, and Hypertrophic Hemangiectases: KTW,
As a
Combined Malformation Disease. Psychiatr. Neurol. Med. Psychol:
Leipz, 18:6, 1966.
Sciubba, J., and A. Brown: Oral-Facial Manifestations of KTW
Syndrome: Report of Two Cases. Oral Surg. Oral Med. Oral Pathol.,
43:2, 1977.
Sehgal, V.,S. Aggarwal, and R. Gupta: KTPW Syndrome. Dermatol Int.,
7:4, 1968.
Seoud, M.,R. Santos-Ramos, and J. Friedman: Early Prenatal Ultrasonic
Findings in KTW Syndrome. Prenat. Diagn., 4:3, 1984.
Servelle, M.: Klippel and Trenaunay's Syndrome: 768 Operated Cases.
Ann. Surg., 2001:3, 1985.
Servelle, M., and J. Babillot: Deep Vein Malformations in the KT
Syndrome. Phlebologie, 33:1, 1980.
Servelle, M., J. Bastin, R., and J. Loygue: Hematuria and Rectal
Bleeding in the Child with KT Syndrome. Ann. Surg., 183:4, 1976.
Servelle, M.,H. Turpyn, and J. Leducq: Malformation of the Thoracic
Duct Associated with the KT Syndrome. Coeur Med. Interne, 5:4,
1966.
Servelle, M.,E. Zolotas, and J. Soulie: KT Syndrome: Malformations of
the Iliac, Femoral and Popliteal Veins. Arch Mal Coeur, 58:8, 1965.
Shalaev, M.,A. Starodumov, and K. Meliuk: A Rare Variant of the KT
Syndrome. Sov Med. 34:3, 1971.
Sharma, P.,A. Arya, and R. Azad: Unusual Retinal Manifestation
in a Combination of Sturge-Weber and KT syndrome-- A Case Report.
Indian Journal of Ophthalmology, 38:4, 1990.
Shih JC, et al.: Application of the surface rendering technique
of three-dimensional ultrasound in prenatal diagnosis and counseling
of Klippel-Trenaunay-Weber syndrome.
Prenat Diagn. 1998 Mar; 1 8(3):298-302.
PMID: 9556049; UI: 98215335.
Shime, H.,R. Araki and H. Koide: A Case of KTW Syndrome
Accompanied by Congenital Hydrocephalus and Micropolygyria .
(Japanese) No To Hattatsu, 24:4, 1992.
Siano, V.,N. Kuklin, and V. Mordokhovich: KT syndrome. Vestn
Dermatol Venerol., 5, 1986.
Siegel, M.: Contribution to the KTW Syndrome. Dermatol Wochenschr,
152:15, 1966.
Silber, R.: Segmental Hemangiomatosis of the Distal Colon in a Patient
with KT Syndrome. Med Welt., 301:12, 1980.
Simkin, R. , C. Esteban, and R. Bulloj: KT syndrome. (French)
Phlebologie, 43:4, 1990.
Snow, R. , and M. Lecklitner: Musculoskeletal findings in KT
syndromeClinical Nuclear Medicine16:12, 1991.
Somasundaram, V.,S. Premalatha, and N. Rao: Hemangiectatic
hypertrophy with angiokeratoma circumscriptum.Int J Dermatol,
27:1, 1988.
Sooriakumaran, S. ,T. Landham: The KT Syndrome. Journal of Bone
and Joint Surgery. (British) Volume, 701:1, 1991.
Spoor, T.,J. Kennerdell, and J. Maroon: Pneumosinus Kilatans, KTW
Syndrome, and Progressive Visual Loss. Ann Ophthalmol, 13:1, 1981.
Srivastava DN. et al.: Klippel-Trenaunay syndrome: unusual
magnetic resonance features. Australas Radiol. 1998 Feb;42(1):88-9.
PMID: 9509616; UI: 98170356.
Stella, A.,M. Gessaroli, and L. Pedrini: Possibilities and Limitations
of
Doppler Flowmeters in the Study of Angiodysplasias of the
Extremities. Angiologia, 38:1, 1986.
Stewart, G., and G. Farmer: Sturge-Weber and KT Syndromes with
Absence of Inferior Vena Cava. Archives of Disease in Childhood,
65:5, 1990.
Stickler, G.: Growth of Cavernous Hemangioma with Puberty: Letter .
Clin. Pediatr. (Phila), 25:12, 1986.
Stone DH, et al. : A unique approach in the management of vena
caval thrombosis in a patient with Klippel-Trenaunay syndrome.
J Vasc Surg. 1997 Jul;26(l):155-9.
PMID: 9240337; UI: 97384669.
Stritzler C, et al.: Cutaneous angiopathy and solitary renal cysts
(coincidental or related?). Arch Dermatol. 1965 Apr;91(4):415-6.
No abstract available.
PMID: 9626102; UI: 98289342.
Suzuki, S., and R. Kikuchi: KTW Syndrome. Rinsho Hoshasen, 15:11,
1970.
Sylvestre, G.,A. Barbeau, and J. Girous: Ota's Nevus Associated with
Multiple Blue Nevi of the Skin and Uterine Cervix, with Ichthyosis
Vulgaris and the KT Syndrome. Union Med Can, 104:9, 1975.
Syzuki, S., R. Kikuchi: KTW Syndrome. Rinsho Hoshasen, 15:11, 1970.
Taguthi, Y., K. Kurata, and N. Maito: Case of KT Syndrome. Seikei Geka,
20:9, 1969.
Taira, T. ,Y. Tamura, and H. Kawamura: Intracranial Aneurysm in a
Child with KTW Syndrome: Case Report. Surgical Neurology, 36:4,
1991.
Tan, E.,T. Takagi, and H. Nagai: Spinal Arteriovenous Malformations
in
KTW Syndrome: Case report.(Japanese) No Shinkei GekaÑNeurological
Surgery, 18:9, 1990.
Tanioka, F.,M. Matsui, and T. Tsubo: Anesthetic Management of
a
Patient with KTW Syndrome. Masui, 32:1, 1983.
Tesier, L., L. Sarrat, and Faberes: On Two cases of KT Syndrome. Bull
Soc Fr Dermatol Syphiligr, 75:1, 1968.
Thiers, J., G. Moulin, and B. Durand: Appearance of Kaposi's Disease
with KT Syndrome. Bull Soc Fr Dermatol Syphiligr, 75:2, 1968.
Tjaden, B.,J. Buscema, and J. Haller: Vulvar Congenital Dysplastic
Angiopathy. Obstetrics & Gynecology, 75:3, 1990.
Telander, R.,B. Kaufman, and P. Gloviczki: Prognosis and Management
of Lesions of the Trunk in Children with KT Syndrome. Journal of
Pediatric Surgery, 19:4, 1984.
Togel, H.: Combination of an Appendix Bifida and KT Syndrome.
Chirurg, 50:6, 1979.
Travis, R.,D. Rowan, and J. Miller: Just Another Case of Varicose
Veins? British Journal of Radiology, 63:751, 1990.
Troncone, S.,A. Beccaria, and A. Girardi :On a Case of Multiple
Arteriovenous Malformations in a Patient with KTPW Syndrome.
Minerva Chir, 42:8, 1966.
Troost, B.,P. Savino, and J. Lozito: Tuberous Sclerosis and KTW
Syndromes: Association of Two Complete Phakomatoses in a Single
Individual. Journal of Neurol Neurosurg Psychiatry, 38:5, 1975.
Trout, J., H. McAllister, and J. Giordano: Vascular Anomalies. J Vasc
Surg, 3:5, 1986.
Ueki, J., Y. Inagake, and M. Kohda: Stewart-Bluefarb syndrome:
Kaposiform Arteriovenous Fistula with Bone Changes. Hautarzt,
37:12, 1986.
Vagner, E.,M. Shalaev, and N. Sushin: The KT Syndrome. Klin Khir, 8,
1968.
Vajda, P., and M. Brozmanova: KT Syndrome with a Developmental
Defect and Hemangioma of the Spinal Cord. Cesk Neurol Neurochir,
46:2, 1983.
Vajo Z, et al.: Picture of the month. Klippel-Trenaunay syndrome.
Arch Pedjatr Adoesc Med. 1998 Nov;152(11):1 149; discussion 1150.
No abstract available.
PMID: 9811297; UI: 99027436.
Valenzano, L., and V. Testa: Association of the KTPW Syndrome with
the Sturge-Weber: 0Krabbe Syndrome. Minerva Dermatol., 42:8,
1967.
Van der Stricht, J.: KT Syndrome and Phacomatoses. Phlebologie, 33:1,
1980.
Van Laere, J.: Familial Progressive Chronic Bulbo-Pontine Paralysis
with Deafness: A Case of KT Syndrome in Siblings of the Same family:
Diagnostic and Genetic Problems. Rev Neurol: Paris, 115:2, 1966.
Vereanu, D.,M. Teodorescu, and Z. Fruchter: Considerations on a Case
of KT Pseudo-Syndrome in a Child. Pediatria: Bucur, 15:4, 1966.
Viljoen, D. : KTW syndrome: Angio-Osteohypertrophy Syndrome. J
Med Genet, 25:4, 1988.
Viljoen, D.,N. Saxe, and J. Pearn: The Cutanious Manifestations
of the
KTW Syndrome: Clin Exp Dermatol, 12:1, 1987.
Villar, M.,L. Del Campo, and B. Galvany: KTW Syndrome. Rev Clin Esp,
156:6, 1980.
Vollmar, J.: History and Terminology of the FP Weber and KT
Syndromes: Review article: 25 refs. Vasa, 3:3, 1974.
Voorhoeve, H.: Two Nigerian Children with the KT Syndrome. Trop
Geogr Med, 201:3, 1969.
Warhit, J.,M. Goldman, and L. Sachs: KTW Syndrome: Appearance
in
Utero. Journal of Ultrasound Med., 2:11, 1983.
Weiner, S.,R. Weiss, and B. Bauthier: Intrarenal Hemangiomas in the
KT Syndrome. Urol Radiol, 7:1, 1985.
Weiss, V.,E. Urtl, and D. Eberhard: Sonographic and Phlebographic
Clarification of an Unclear Swelling in the Mons Pubis Area. ROFO,
147:5, 1987.
Williams, D., and A. Elster: Cranial CT and MR in the KTWSsyndrome.
American Journal of Neuroradiology, 13:1, 1992.
Wortzel, M.: The KTPW Syndrome. J Med Soc NJ, 63:9, 1966.
Xu, J.: Radiological Manifestations and Classification of Venous
Diseases of the Lower Limbs: An Analysis of Ascending Venography
of 675 Extremities. Chung Hua Fang She Hsueh Tsa Chih, 201:3, 1987.
Yang CB, et al.: Use of latanoprost in the treatment of glaucoma
associated with Sturge-Weber syndrome.
Am J Ophthalmol. 1998 Oct;126(4):600-2.
PMID: 9780111; UI: 98451391.
You, C.,J. Rees, and D. Gillis: KT syndrome: A Review.
Can J Surg., 26:5,1983.
Young SA, et al.: Klippel-Trenaunay-Weber syndrome with adrenal
pseudocyst: characterization by blood pool and adrenocortical
iodocholesterol scintigraphy.
Clin Nucl Med. 1998 Aug;23(8):528-31.
PMID: 9712387; UI: 98376232
Yousem, D.,W. Scott, and E. Fishman: Case Report 440:
KT Syndrome of the Right Lower Extremity. Skeletal Radiol.,
16:8, 1987.
Yusta, I ,C. Villagra, and T. Perez: Hemorrhage of the Encephalic
Trunk in a Patient with the KT Syndrome: Letter (Spanish) Revista
Clinica Espanola, 187:1, 1990.
Zabel, J., and Z. Daras: Case of Parkes Weber Syndrome. Przeql
Dermatol, 65:3, 1978.
ZamiraNazara, S.,A. Paredes, and A. Hernandez: KTW Syndrome. Bol
Med Hosp Infant Mex, 301:5, 1974.
Zeller, J.,A. Hovnanian, and Y. Raulo: A Case of Proteus Syndrome
(French) Annales De Dematologie Et De Venereologie, 118:11, 1991.
Zwierzchowska, D.,M. Spodenkiewicz,: KT Disease. Chir Narzadow
Ruchu Ortop Pol, 46:3, 1981.
Case of the month: KTW syndrome. Indian Pediatr, 16:12, 1979.
KT or Parkes Weber. (Trans) St. Johns Hosp Dermatol Soc., 52:2, 1966.
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