18
Views
22
CrossRef citations to date
0
Altmetric
Original Article

Neu-Laxova Syndrome: Report of Two Cases

, , &
Pages 295-306 | Received 13 Jan 1984, Accepted 11 Feb 1985, Published online: 09 Jul 2009

References

  • Neu R L, Kajii T, Gardner L I, Nagyfy S F, King S. A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings. Pediatrics 1971; 47: 610–612
  • Laxova R, O'Hara P T, Timothy JAD. A further example of a lethal autosomal recessive condition in sibs. J. Vent Defic Res 1972; 16: 139–143
  • Povysilova V, Macek M, Salichova J, Seemanova E. Letalni sundrom mnohocetnych malformaci u tre sourozencu. Ces Pediatr 1976; 31: 190–194
  • Lazjuk G I, Lurie I W, Ostrowskaja T I, et al. Brief clinical observations: The Neu-Laxova syndrome-A distinct entity. Am J Med Genet 1979; 3: 261–267
  • Winter R M, Donnai D, d'A Crawfurd M. Syndromes jof microcephaly, microphthalmia, cataracts, and joint contractures. J Med Genet 1981; 18: 129–133
  • Scott C, Louro J, Lawrence K, et al. Letter to the Editor: Comments on the Neu-Laxova syndrome and the CAD complex. Am J Med Genet 1981; 9: 165–175
  • Fitch N, Resch L, Rochon L. The Neu-Laxova syndrome: Comments on syndrome identification. Am J Med Genet 1982; 13: 445–452
  • Scott-Emudkpor A, Heffelfinger J, Higgins J. A syndrome of microcephaly and cataracts in four siblings. Am J Dis Child 1977; 131: 167–169
  • Pena S DJ, Evans J, Hunter A GW. COPS syndrome revisited. Recent Advances and New Syndromes, D. Bergsma. Alan R. Liss for the National Foundation-March of Dimes. 1978; 205–213
  • Cohen MJ, Jr. On the nature of syndrome delineation. Acta Genet Med Gemellol 1977; 26: 103–119
  • Curry C, JR. Letter to the Editor: Further comments on the Neu-Laxova syndrome. Am J Med Genet 1981; 13: 441–444
  • Fitch N, Curry C, JR. Letter to the Editor: Comments on Dr. Curry's classification of the Neu-Laxova syndrome. Am J Med Genet 1983; 15: 515–517
  • Reynolds D J, Marks R, Davies M G, Dykes PJ. The fatty acid composition of skin and plasma lipids in Refsum's disease. Clin Chim Acta 1978; 90: 171
  • Shapiro LJ. Steroid sulfatase deficiency and X-linked ichthyosis. The Metabolic Basis of Inherited Disease, J. B. Stanbury, et al. McGraw-Hill, New York 1983; 1034
  • Lowe N J, Stoughton RB. Essential fatty acid deficient hairless mouse: A model of chronic epidermal hyperproliferation. Br J Dermatol 1977; 96: 155
  • Anton-Lamprecht I. Zur Ultrastructur Hereditarer Verhornungsstorungen: U Ichthyosis Bein Refsum Syndrome. Arch Dermatol Forsch 1974; 250: 185
  • Williams M L, Elias PM. X-linked ichthyosis: Elevated cholesterol sulfate in pathologic stratum corneum. Clin Res 1981; 29: 26
  • Buxman M M, Goodkin P E, Fahrenbach W H, Dimond RL (1979). Harlequin ichthyosis with epidermal lipid abnormality. Arch Dermatol 1979; 115: 189
  • Winkelmann R K, Perry H O, Achor RU. Cutaneous syndromes produced as side effects of triparanol therapy. Arch Dermatol 1963; 87: 372
  • Flesch P. Inhibition of kerdtinizing structures by systemic drugs. Pharmacol Rev 1963; 15: 653
  • Lever W F, Schaumburg-Lever G. Histopathy of the Skin5th ed. J. B. Lippincott, Philadelphia 1975; 411–412
  • Shved I A, Lazjuk G I, Cberstvoy ED. Elaboration of the phenotypic: changes of the upper limbs in the Neu-Laxova syndrome. Am J Med Genet 1985; 20: 1–11
  • Turkel S B, Ebbin A J, Towner JW. Additional manifestations of the Neu-Laxova syndrome. J Med Genet 1983; 20: 227–229
  • Scemanova E, Rudolf R. Letter to the Editor: The Neu-Laxova syndrome. Am J Med Genet 1985; 20: 13–15

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.