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2. Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: report of a brother and sister from Turkey. Oğur G; Yüksel-Apak M; Demiryont M Am J Med Genet; 1990 Sep; 37(1):6-9. PubMed ID: 1700609 [TBL] [Abstract][Full Text] [Related]
3. Congenital cutis laxa with retardation of growth and motor development: a recessive disorder of connective tissue with male lethality. Allanson J; Austin W; Hecht F Clin Genet; 1986 Feb; 29(2):133-6. PubMed ID: 2420495 [TBL] [Abstract][Full Text] [Related]
4. Congenital cutis laxa with retardation of growth and development. Patton MA; Tolmie J; Ruthnum P; Bamforth S; Baraitser M; Pembrey M J Med Genet; 1987 Sep; 24(9):556-61. PubMed ID: 3669050 [TBL] [Abstract][Full Text] [Related]
5. Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defects. Biver A; De Rijcke S; Toppet V; Ledoux-Corbusier M; Van Maldergem L Clin Genet; 1994 Jun; 45(6):318-22. PubMed ID: 7523003 [TBL] [Abstract][Full Text] [Related]
6. Cutis laxa, intrauterine growth retardation, and bilateral dislocation of the hips: a report of five cases. Karrar ZA; Elidrissy AT; Adam KA Prog Clin Biol Res; 1982; 104():215-22. PubMed ID: 6891788 [TBL] [Abstract][Full Text] [Related]
7. Defective protein glycosylation in patients with cutis laxa syndrome. Morava E; Wopereis S; Coucke P; Gillessen-Kaesbach G; Voit T; Smeitink J; Wevers R; Grünewald S Eur J Hum Genet; 2005 Apr; 13(4):414-21. PubMed ID: 15657616 [TBL] [Abstract][Full Text] [Related]
8. Cutis laxa associated with central hypothyroidism owing to isolated thyrotropin deficiency in a newborn. Koklu E; Gunes T; Ozturk MA; Akcakus M; Buyukkayhan D; Kurtoglu S Pediatr Dermatol; 2007; 24(5):525-8. PubMed ID: 17958802 [TBL] [Abstract][Full Text] [Related]
9. Selected disorders of connective tissue: pseudoxanthoma elasticum, cutis laxa, and lipoid proteinosis. Ringpfeil F Clin Dermatol; 2005; 23(1):41-6. PubMed ID: 15708288 [TBL] [Abstract][Full Text] [Related]
10. Cutis laxa type II and wrinkly skin syndrome: distinct phenotypes. Gupta N; Phadke SR Pediatr Dermatol; 2006; 23(3):225-30. PubMed ID: 16780467 [TBL] [Abstract][Full Text] [Related]
11. [Cutis laxa syndrome associated with articular calcification punctata]. Mula García JA; Castro García FJ; Gutiérrez-Macías A; Peris Mencheta MD; Rodríguez Penalver M An Esp Pediatr; 1989 May; 30(5):372-6. PubMed ID: 2667411 [TBL] [Abstract][Full Text] [Related]
12. Congenital athetosis, mental deficiency, dwarfism and laxity of skin and ligaments. Hoefnagel D; Pomeroy J; Wurster D; Saxon A Helv Paediatr Acta; 1971 Oct; 26(4):397-402. PubMed ID: 5123306 [No Abstract] [Full Text] [Related]
14. Decreased bone density and treatment in patients with autosomal recessive cutis laxa. Noordam C; Funke S; Knoers NV; Jira P; Wevers RA; Urban Z; Morava E Acta Paediatr; 2009 Mar; 98(3):490-4. PubMed ID: 19055655 [TBL] [Abstract][Full Text] [Related]
15. [Surgical treatment of skin changes in cutis laxa (author's transl)]. Breitbart E; Mensing H; Meigel W Z Hautkr; 1981 Jan; 56(2):90-7. PubMed ID: 7222885 [TBL] [Abstract][Full Text] [Related]
16. Cutis laxa associated with severe intrauterine growth retardation and congenital dislocation of the hip. Reisner SH; Seelenfreund M; Ben-Bassat M Acta Paediatr Scand; 1971 May; 60(3):357-60. PubMed ID: 5579863 [No Abstract] [Full Text] [Related]
17. A novel elastin gene mutation resulting in an autosomal dominant form of cutis laxa. Rodriguez-Revenga L; Iranzo P; Badenas C; Puig S; Carrió A; Milà M Arch Dermatol; 2004 Sep; 140(9):1135-9. PubMed ID: 15381555 [TBL] [Abstract][Full Text] [Related]
18. Congenital cutis laxa syndrome: type II autosomal recessive inheritance. Tüysüz B; Arapoğlu M; Ilikkan B; Demirkesen C; Perk Y Turk J Pediatr; 2003; 45(3):265-8. PubMed ID: 14696810 [TBL] [Abstract][Full Text] [Related]
19. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833 [TBL] [Abstract][Full Text] [Related]