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J Med Genet. 1990 March; 27(3): 180–187.
PMCID: PMC1017001

Focal dermal hypoplasia (Goltz syndrome).

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • GORLIN RJ, MESKIN LH, PETERSON WC, Jr, GOLTZ RW. FOCAL DERMAL HYPOPLASIA SYNDROME. Acta Derm Venereol. 1963;43:421–440. [PubMed]
  • Hall EH, Terezhalmy GT. Focal dermal hypoplasia syndrome. Case report and literature review. J Am Acad Dermatol. 1983 Sep;9(3):443–451. [PubMed]
  • Wettke-Schäfer R, Kantner G. X-linked dominant inherited diseases with lethality in hemizygous males. Hum Genet. 1983;64(1):1–23. [PubMed]
  • Goltz RW, Henderson RR, Hitch JM, Ott JE. Focal dermal hypoplasia syndrome. A review of the literature and report of two cases. Arch Dermatol. 1970 Jan;101(1):1–11. [PubMed]
  • Warburg M. Focal dermal hypoplasia. Ocular and general manifestations with a survey of the literature. Acta Ophthalmol (Copenh) 1970;48(3):525–536. [PubMed]
  • Aymé S, Fraser FC. Possible examples of the goltz syndrome (focal dermal hypoplasia) without linear areas of skin hypoplasia. Birth Defects Orig Artic Ser. 1982;18(3B):59–65. [PubMed]
  • Jackson R. The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skin. Br J Dermatol. 1976 Oct;95(4):349–360. [PubMed]
  • Brinson RR, Schuman BM, Mills LR, Thigpen S, Freedman S. Multiple squamous papillomas of the esophagus associated with Goltz syndrome. Am J Gastroenterol. 1987 Nov;82(11):1177–1179. [PubMed]
  • Tsuji T. Focal dermal hypoplasia syndrome. An electron microscopical study of the skin lesions. J Cutan Pathol. 1982 Aug;9(4):271–281. [PubMed]
  • Uitto J, Bauer EA, Santa-Cruz DJ, Loewinger RJ, Eisen AZ. Focal dermal hypoplasia: abnormal growth characteristics of skin fibroblasts in culture. J Invest Dermatol. 1980 Aug;75(2):170–175. [PubMed]
  • Ureles SD, Needleman HL. Focal dermal hypoplasia syndrome (Goltz syndrome): the first dental case report. Pediatr Dent. 1986 Sep;8(3):239–244. [PubMed]
  • Temple IK, Hurst JA, Hing S, Butler L, Baraitser M. De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies. J Med Genet. 1990 Jan;27(1):56–58. [PMC free article] [PubMed]
  • Fryns JP, Dhondt F, Lindemans L, Van den Berghe H. Focal dermal hypoplasia (Goltz syndrome) in a male. Acta Paediatr Belg. 1978 Jan-Mar;31(1):37–39. [PubMed]
  • WODNIANSKY P. Uber die Formen der congenitalen Poikilodermie. Arch Klin Exp Dermatol. 1957;205(4):331–342. [PubMed]
  • Atherton DJ, Hall M. Focal dermal hypoplasia syndrome. Clin Exp Dermatol. 1980 Jun;5(2):249–252. [PubMed]
  • Burgdorf WH, Dick GF, Soderberg MD, Goltz RW. Focal dermal hypoplasia in a father and daughter. J Am Acad Dermatol. 1981 Mar;4(3):273–277. [PubMed]
  • Ruiz-Maldonado R, Carnevale A, Tamayo L, Milonas de Montiel M. Focal dermal hypoplasia. Clin Genet. 1974;6(1):36–45. [PubMed]
  • Wechsler MA, Papa CM, Haberman F, Marion RW. Variable expression in focal dermal hypoplasia. An example of differential X-chromosome inactivation. Am J Dis Child. 1988 Mar;142(3):297–300. [PubMed]
  • Happle R, Lenz W. Striation of bones in focal dermal hypoplasia: manifestation of functional mosaicism? Br J Dermatol. 1977 Feb;96(2):133–135. [PubMed]

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