Indexed keywords
ADULT;
ARTICLE;
CASE REPORT;
CONGENITAL HIP DISLOCATION;
CUTIS LAXA;
ELECTROCARDIOGRAM;
FEMALE;
GROWTH RETARDATION;
HEART VENTRICLE SEPTUM DEFECT;
HUMAN;
HUMAN TISSUE;
JOINT CONTRACTURE;
KYPHOSCOLIOSIS;
LABORATORY TEST;
MALE;
PHENOTYPE;
PHYSICAL EXAMINATION;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
SKIN BIOPSY;
SKIN MANIFESTATION;
UMBILICAL HERNIA;
VAGINAL DELIVERY;
CHILD, PRESCHOOL;
CUTIS LAXA;
FACIES;
FEMALE;
HUMANS;
INDIA;
ISLAM;
MALE;
PHENOTYPE;
SKIN AGING;
SYNDROME;
1
0015061638
Cutis laxa associated with severe intrauterine growth retardation and congenital dislocation of hip
Reisner SH Seelanfreund M Ben BM. Cutis laxa associated with severe intrauterine growth retardation and congenital dislocation of hip. Acta Pediatr Scand 1971 60: 357 360.
(1971)
Acta Pediatr Scand , vol.60
, pp. 357-360
Reisner, S.H.1
Seelanfreund, M.2
Ben, B.M.3
2
0021021961
Syndrome of cutis laxa, ligamentous laxity, and delayed development
Sakati NO Nyhan WL Shear CS et al. Syndrome of cutis laxa, ligamentous laxity, and delayed development. Pediatrics 1983 72: 850 856.
(1983)
Pediatrics , vol.72
, pp. 850-856
Sakati, N.O.1
Nyhan, W.L.2
Shear, C.S.3
3
0015888456
The wrinkly skin syndrome: A new heritable disorder of connective tissue
Gazit E Goodman RM Bat M et al. The wrinkly skin syndrome: a new heritable disorder of connective tissue. Clin Genet 1973 4: 186 192.
(1973)
Clin Genet , vol.4
, pp. 186-192
Gazit, E.1
Goodman, R.M.2
Bat, M.3
4
0020611640
The wrinkly skin syndrome: A report of two siblings from Saudi Arabia
Karrar ZA Elidrissy ATH Al Arabi K et al. The wrinkly skin syndrome: a report of two siblings from Saudi Arabia. Clin Genet 1983 23: 308 310.
(1983)
Clin Genet , vol.23
, pp. 308-310
Karrar, Z.A.1
Elidrissy, A.T.H.2
Al Arabi, K.3
5
30644466293
Cutis laxa retarded development and joint hyper mobility syndrome
Goldblatt J Wallis C Viljoen D et al. Cutis laxa retarded development and joint hyper mobility syndrome. Dysmorph Clin Genet 1988 1: 142 144.
(1988)
Dysmorph Clin Genet , vol.1
, pp. 142-144
Goldblatt, J.1
Wallis, C.2
Viljoen, D.3
6
0028144305
Male with type II autosomal recessive cutis laxa
Imaizumi K Kurosawa K Makita Y et al. Male with type II autosomal recessive cutis laxa. Clin Genet 1994 45: 40 43.
(1994)
Clin Genet , vol.45
, pp. 40-43
Imaizumi, K.1
Kurosawa, K.2
Makita, Y.3
7
0025143047
Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: Report of a brother and sister from Turkey
Ogur G Yuksel-Apak M Demiryont M. Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: report of a brother and sister from Turkey. Am J Med Genet 1990 37: 6 9.
(1990)
Am J Med Genet , vol.37
, pp. 6-9
Ogur, G.1
Yuksel-Apak, M.2
Demiryont, M.3
8
0032999953
Wrinkly skin syndrome and the syndrome of cutis laxa with growth and developmental delay represent the same disorder (Letter)
Zlotgora J. Wrinkly skin syndrome and the syndrome of cutis laxa with growth and developmental delay represent the same disorder (Letter). Am J Med Genet 1999 85: 194.
(1999)
Am J Med Genet , vol.85
, pp. 194
Zlotgora, J.1
9
0032944144
Neurological involvement in a child with the wrinkly skin syndrome
Azuri J Mizrachi A Weintraub S et al. Neurological involvement in a child with the wrinkly skin syndrome. Am J Med Genet 1999 82: 31 33.
(1999)
Am J Med Genet , vol.82
, pp. 31-33
Azuri, J.1
Mizrachi, A.2
Weintraub, S.3
10
0023634690
Wrinkly skin syndrome: Phenotype and additional manifestations
Casamassima AC Wesson SK Conlon CJ et al. Wrinkly skin syndrome: Phenotype and additional manifestations. Am J Med Genet 1987 27: 885 893.
(1987)
Am J Med Genet , vol.27
, pp. 885-893
Casamassima, A.C.1
Wesson, S.K.2
Conlon, C.J.3
