169 related articles for article (PubMed ID: 2420495)
41. Cutis laxa with delayed development.
Rogers JG; Danks DM
Aust Paediatr J; 1985 Nov; 21(4):281-3. PubMed ID: 4091771
[TBL] [Abstract][Full Text] [Related]
42. Congenital cutis laxa syndrome: relation of joint dislocations to oligohydramnios.
Gardner LI; Sanders-Fay K; Bifano EM
Arch Dermatol; 1986 Nov; 122(11):1241-3. PubMed ID: 3777971
[No Abstract] [Full Text] [Related]
43. Cutis Laxa.
Mohamed M; Voet M; Gardeitchik T; Morava E
Adv Exp Med Biol; 2014; 802():161-84. PubMed ID: 24443027
[TBL] [Abstract][Full Text] [Related]
44. Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype.
Elahi E; Kalhor R; Banihosseini SS; Torabi N; Pour-Jafari H; Houshmand M; Amini SS; Ramezani A; Loeys B
J Invest Dermatol; 2006 Jul; 126(7):1506-9. PubMed ID: 16691202
[TBL] [Abstract][Full Text] [Related]
45. [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]
46. Loss-of-Function Variants in
Verlee M; Beyens A; Gezdirici A; Gulec EY; Pottie L; De Feyter S; Vanhooydonck M; Tapaneeyaphan P; Symoens S; Callewaert B
Genes (Basel); 2021 Mar; 12(4):. PubMed ID: 33807164
[TBL] [Abstract][Full Text] [Related]
47. Congenital Cutis Laxa Type 2 Associated With Recurrent Aspiration Pneumonia and Growth Delay: Case Report.
Rahmati M; Yazdanparast M; Jahanshahi K; Zakeri M
Electron Physician; 2015 Oct; 7(6):1391-3. PubMed ID: 26516448
[TBL] [Abstract][Full Text] [Related]
48. Type II autosomal recessive cutis laxa: report of another patient and molecular studies concerning three candidate genes.
Scherrer DZ; Alexandrino F; Cintra ML; Sartorato EL; Steiner CE
Am J Med Genet A; 2008 Nov; 146A(21):2740-5. PubMed ID: 18819152
[TBL] [Abstract][Full Text] [Related]
49. 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]
50. A novel deletion mutation in the ATP6V0A2 gene in an Iranian patient affected by autosomal recessive cutis laxa.
Shafagh Shishavan N; Morovvati S
Ir J Med Sci; 2023 Oct; 192(5):2279-2282. PubMed ID: 36520350
[TBL] [Abstract][Full Text] [Related]
51. Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family.
Tekedereli I; Demiral E; Gokce IK; Esener Z; Camtosun E; Akinci A
Clin Dysmorphol; 2019 Apr; 28(2):63-65. PubMed ID: 30640789
[TBL] [Abstract][Full Text] [Related]
52. Cutis laxa.
George S; Jacob M; Pulimood S; Chandi SM
Clin Exp Dermatol; 1998 Sep; 23(5):211-3. PubMed ID: 10233603
[TBL] [Abstract][Full Text] [Related]
53. First report of a short in-frame biallelic deletion removing part of the EGF-like domain calcium-binding motif in LTBP4 and causing autosomal recessive cutis laxa type 1C.
Ravel JM; Comel M; Wandzel M; Bronner M; Tatopoulos A; Renaud M; Lambert L; Bursztejn AC; Bonnet C
Am J Med Genet A; 2022 Nov; 188(11):3343-3349. PubMed ID: 35972031
[TBL] [Abstract][Full Text] [Related]
54. A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance.
Dallaire L; Cantin M; Melançon SB; Perreault G; Potier M
Clin Genet; 1976 Jul; 10(1):1-11. PubMed ID: 949858
[TBL] [Abstract][Full Text] [Related]
55. Clinical and molecular characterization of an 18-month-old infant with autosomal recessive cutis laxa type 1C due to a novel LTBP4 pathogenic variant, and literature review.
Ritelli M; Cammarata-Scalisi F; Cinquina V; Colombi M
Mol Genet Genomic Med; 2019 Jul; 7(7):e00735. PubMed ID: 31115174
[TBL] [Abstract][Full Text] [Related]
56. Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibs.
Van Maldergem L; Vamos E; Liebaers I; Petit P; Vandevelde G; Simonis-Blumenfrucht A; Bouffioux R; Kulakowski S; Hanquinet S; Van Durme P
Am J Med Genet; 1988 Oct; 31(2):455-64. PubMed ID: 3232707
[TBL] [Abstract][Full Text] [Related]
57. Cutis laxa: case report.
Nascimento GM; Nunes CS; Menegotto PF; Raskin S; Almeida Nd
An Bras Dermatol; 2010; 85(5):684-6. PubMed ID: 21152794
[TBL] [Abstract][Full Text] [Related]
58. Congenital cutis laxa and lysyl oxidase deficiency.
Khakoo A; Thomas R; Trompeter R; Duffy P; Price R; Pope FM
Clin Genet; 1997 Feb; 51(2):109-14. PubMed ID: 9111998
[TBL] [Abstract][Full Text] [Related]
59. 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]
60. [Cutis laxa. Classification, clinical aspects and molecular defects].
Mensing H; Krieg T; Meigel W; Braun-Falco O
Hautarzt; 1984 Oct; 35(10):506-11. PubMed ID: 6500933
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
