Wrinkly skin syndrome: Phenotype and additional manifestations

The wrinkly skin syndrome is an autosomal recessive disorder characterized by wrinkling of the skin of the dorsum of the hands and feet, decreased elastic recoil of the skin, an increased number of palmar and plantar creases, multiple musculoskeletal abnormalities, microcephaly, and mental retardation. Our patient is characteristic of the syndrome as previously described, and confirms the presence of mental retardation and microcephaly as component manifestations, with the additional findings of connective tissue abnormalities evidenced by an atrial septal aneurysm.

[1]  M. C. Brunazzi,et al.  Atrial septal aneurysm: echopolycardiographic study. , 1985, The American journal of cardiology.

[2]  J. Rosenbloom,et al.  Chromosomal localization of the human elastin gene. , 1985, American journal of human genetics.

[3]  M. Malergue,et al.  Atrial septal aneurysm--a potential cause of systemic embolism. An echocardiographic study. , 1985, British heart journal.

[4]  S. Iliceto,et al.  Combined atrial septal aneurysm and mitral valve prolapse: detection by two-dimensional echocardiography. , 1984, The American journal of cardiology.

[5]  W. Roberts Aneurysm (redundancy) of the atrial septum (fossa ovale membrane) and prolapse (redundancy) of the mitral valve. , 1984, The American journal of cardiology.

[6]  S. Iliceto,et al.  Detection of atrial septal defect by right sternal border echocardiography. , 1984, The American journal of cardiology.

[7]  D. Duksin,et al.  Altered protein glycosylation and procollagen to collagen conversion in human fibroblasts. , 1983, Laboratory investigation; a journal of technical methods and pathology.

[8]  Z. Karrar,et al.  The wrinkly skin syndrome: A report of two siblings from Saudi Arabia , 1983, Clinical genetics.

[9]  R. Reder,et al.  Aneurysm of the interatrial septum causing pulmonary venous obstruction in an infant with tricuspid atresia. , 1981, American heart journal.

[10]  N. Nanda,et al.  Two-dimensional echocardiographic features of atrial septal aneurysms. , 1981, Circulation.

[11]  W. Groot,et al.  Familial acrogeria (Gottron) , 1980, The British journal of dermatology.

[12]  K. Jones,et al.  TWO FORMS OF CUTIS LAXA PRESENTING IN THE NEWBORN PERIOD , 1978, Acta paediatrica Scandinavica.

[13]  D. Hollister Heritable disorders of connective tissue: Ehlers-Danlos syndrome. , 1978, Pediatric clinics of North America.

[14]  R. Ross,et al.  Fine structure alterations of elastic fibers in pseudoxanthoma elasticum , 1978, Clinical genetics.

[15]  S. Goldberg,et al.  Echocardiographic diagnosis of atrial septal aneurysm in an infant with hypoplastic right heart syndrome. , 1978, Chest.

[16]  Dorsey Js Aneurysms of the septum primum in adults. , 1978 .

[17]  R. Rowe,et al.  Aneurysm of the atrial septum in tricuspid atresia: diagnosis during life and therapy. , 1976, The American journal of cardiology.

[18]  G. Perreault,et al.  A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance , 1976, Clinical genetics.

[19]  K. Hashimoto,et al.  Cutis laxa. Ultrastructural and biochemical studies. , 1975 .

[20]  F. Pope Historical evidence for the genetic heterogeneity of pseudoxanthoma elasticum , 1975, The British journal of dermatology.

[21]  E. Gazit,et al.  The Wrinkly Skin Syndrome: A new heritable disorder of connective tissue , 1973, Clinical genetics.

[22]  P. Beighton The dominant and recessive forms of cutis laxa. , 1972, Journal of medical genetics.

[23]  K. Melmon,et al.  Pseudotumor of the right atrium. Report of a case and review of its etiology. , 1966, Annals of internal medicine.

[24]  M. Hertz,et al.  The wrinkly skin syndrome and cartilage-hair hypoplasia (a new variant?) in sibs of the same family. , 1982, Progress in clinical and biological research.

[25]  Z. Karrar,et al.  Cutis laxa, intrauterine growth retardation, and bilateral dislocation of the hips: a report of five cases. , 1982, Progress in clinical and biological research.

[26]  O. Mutchinick,et al.  Gerodermia osteodysplastica hereditaria: report of three affected brothers and literature review. , 1979, American journal of medical genetics.