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Indian Journal of Dermatology, Venereology and Leprology

Volumn 74, Issue 1, 2008, Pages 81-

Camisa disease: A rare variant of Vohwinkel's syndrome [11]

(4) Rajashekar, T a Singh, Gurcharan a Naik, Chandra a Okade, Rajendra a

a SRI DEVARAJ URS MEDICAL COLLEGE (India)

Author keywords

[No Author keywords available]

Indexed keywords

ABDOMINAL RADIOGRAPHY; ACANTHOSIS; ANAMNESIS; AUDIOGRAPHY; CAMISA DISEASE; CASE REPORT; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; DISEASE DURATION; EOSINOPHILIA; EYE EXAMINATION; FEMALE; FOOT SOLE; GENETIC DISORDER; HAIR GROWTH; HAND PALM; HEPATOMEGALY; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; ICHTHYOSIS; IRON DEFICIENCY ANEMIA; KERATODERMA HEREDITARIUM MUTILANS; LETTER; LYMPHOCYTIC INFILTRATION; MOUTH EXAMINATION; NAIL DYSTROPHY; PARAKERATOSIS; PRESCHOOL CHILD; SKIN BIOPSY; SKIN DISEASE; TOE;

EID: 38349080786 PISSN: 03786323 EISSN: None Source Type: Journal
DOI: 10.4103/0378-6323.38434 Document Type: Letter

Times cited : (4)

References (6)

1
- 0021174720
- Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin
- Camisa C, Rossano C. Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin. Arch Dermatol 1984;120:1323-8.
- (1984) Arch Dermatol , vol.120 , pp. 1323-1328
- Camisa, C.¹ Rossano, C.²

2
- 0035116593
- Vohwinkel's syndrome in three generations
- Solis RR, Diven DG, Trizna Z. Vohwinkel's syndrome in three generations. J Am Acad Dermatol 2001;44:376-8.
- (2001) J Am Acad Dermatol , vol.44 , pp. 376-378
- Solis, R.R.¹ Diven, D.G.² Trizna, Z.³

3
- 0030846028
- Loricrin mutation in Vohwinkel' keratoderma is unique to the variant with ichthyosis
- Korge BP, Ishida-Yamamoto A, Pünter C, Dopping-Hepenstal PJ, Iizuka H, Stephenson A, et al. Loricrin mutation in Vohwinkel' keratoderma is unique to the variant with ichthyosis. J Invest Dermatol 1997;109:604-10.
- (1997) J Invest Dermatol , vol.109 , pp. 604-610
- Korge, B.P.¹ Ishida-Yamamoto, A.² Pünter, C.³ Dopping-Hepenstal, P.J.⁴ Iizuka, H.⁵ Stephenson, A.⁶

4
- 0032890230
- Loricrin gene mutation in a Japanese patient of Vohwinkel's syndrome
- Takahashi H, Ishida-Yamamoto A, Kishi A, Ohara K, Iizuka H. Loricrin gene mutation in a Japanese patient of Vohwinkel's syndrome. J Dermatol Sci 1999;19:44-7.
- (1999) J Dermatol Sci , vol.19 , pp. 44-47
- Takahashi, H.¹ Ishida-Yamamoto, A.² Kishi, A.³ Ohara, K.⁴ Iizuka, H.⁵

5
- 15844391073
- A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's symdrome
- Maestrini E, Monaco AP, McGrath JA, Ishida-Yamamoto A, Camisa C, Hovnanian A, et al. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's symdrome. Nat Genet 1996;13:70-7.
- (1996) Nat Genet , vol.13 , pp. 70-77
- Maestrini, E.¹ Monaco, A.P.² McGrath, J.A.³ Ishida-Yamamoto, A.⁴ Camisa, C.⁵ Hovnanian, A.⁶

6
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- Variant of Vohwinkel's syndrome
- Ali MM, Upadya GM. Variant of Vohwinkel's syndrome. Indian J Dermatol Venereol Leprol 2006;72:449-51.
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- Ali, M.M.¹ Upadya, G.M.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.