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3. 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]
4. [Outcome of a case of cutis laxa in a infant]. Beer F; Lambert D; Dauvergne M Ann Dermatol Venereol; 1993; 120(12):909. PubMed ID: 8074355 [No Abstract] [Full Text] [Related]
5. [Cutis laxa. Apropos of 2 cases evident in newborn infants]. Khaldi F; Ben Ghachem M; Bahloul H; Saidane T; Trabelsi M; Bouguerra F; Bennaceur B Ann Pediatr (Paris); 1987 Feb; 34(2):165-8. PubMed ID: 3579153 [No Abstract] [Full Text] [Related]
6. [Cutis laxa syndrome. Case report]. Kermane A; Tachfouti S; Lezrek M; Mohcine Z Bull Soc Belge Ophtalmol; 2004; (292):5-8. PubMed ID: 15253484 [TBL] [Abstract][Full Text] [Related]
10. Alimentary bleeding in cutis laxa of late onset. Thaning O; Beighton P S Afr Med J; 1972 Jul; 46(27):928-30. PubMed ID: 4538334 [No Abstract] [Full Text] [Related]
11. Cutis laxa with frontoparietal cortical malformation: a novel type of congenital disorder of glycosylation. Okanishi T; Saito Y; Yuasa I; Miura M; Nagata I; Maegaki Y; Ohno K Eur J Paediatr Neurol; 2008 May; 12(3):262-5. PubMed ID: 18187349 [TBL] [Abstract][Full Text] [Related]
12. [Congenital cutis laxa. A case report with an electron microscopic study]. Sauviat C; Durepaire RM; Cesarini JP; Borde M Ann Pediatr (Paris); 1978 Sep; 25(7):355-61. PubMed ID: 16114347 [No Abstract] [Full Text] [Related]
13. The radiographic findings in congenital cutis laxa. Meine F; Grossman H; Forman W; Jackson D Radiology; 1974 Dec; 113(3):687-90. PubMed ID: 4215097 [No Abstract] [Full Text] [Related]
18. [A case of cutis laxa with high stature]. Okada S; Mori M; Yamada M; Kogure M; Nagasawa T; Kobayashi S Nihon Naika Gakkai Zasshi; 1986 Apr; 75(4):576-81. PubMed ID: 3734548 [No Abstract] [Full Text] [Related]
19. Orthodontic treatment for a patient with congenital cutis laxa. Carrillo R; Rossouw PE Am J Orthod Dentofacial Orthop; 2009 Aug; 136(2):282-9. PubMed ID: 19651360 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]