New progeroid disorder

American Journal of Medical Genetics

Volumn 69, Issue 2, 1997, Pages 182-187

  Penttinen, Maila ^a   Niemi, Kirsti Maria ^b   Vinkka Puhakka, Heli ^c   Johansson, Reijo ^a   Aula, Pertti ^d  

^a TURKU UNIVERSITY HOSPITAL   (Finland)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c UNIVERSITY OF TURKU   (Finland)

^d UNIVERSITY OF TURKU   (Finland)

Author keywords

aero osteolysis; brachydaetyly; delayed closure of anterior fontanel; delayed dentition; prematurely old appearance; skin nodules

Indexed keywords

ACROOSTEOLYSIS; ANTERIOR FONTANEL; ARTICLE; BONE MATURATION; BRACHYDACTYLY; CASE REPORT; CLINICAL FEATURE; FIBROMATOSIS; HUMAN; MALE; PREMATURE AGING; PRIORITY JOURNAL; PROGERIA; SCHOOL CHILD; SKIN BIOPSY; TOOTH DEVELOPMENT;

ABNORMALITIES, MULTIPLE; BIOPSY; CHILD; HUMANS; MALE; MICROSCOPY, ELECTRON; PHENOTYPE; PROGERIA; SKIN; SKIN AGING; SYNDROME; X-RAYS;

EID: 0031052449     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970317)69:2<182::AID-AJMG13>3.0.CO;2-H     Document Type: Article

References (27)

1. Collins P, Barnes L, McCabe M (1991): Poikiloderma congenitale: Case report and review of the literature. Pediatr Dermatol 8(1):58-60.
2. De Barsy AM, Moeus E, Dierchx L (1968): Dwarfism, oligophrenia and degeneration of the elastic tissue in skin and cornea: A new syndrome? Helv Paediatr Acta 3:305-313.
3. De Busk FL (1972): The Hutchinson-Gilford progeria syndrome: Report of 4 cases and review of the literature. J Paediatr 80:697-724.
4. Drescher E, Woyke S, Markiewicz C, Tegi S (1967): Juvenile fibromatosis in siblings (Fibromatosis hyalinica multiplex juvenilis). J Pediatr Surg 2:427-430.
5. Fayad MN, Yacoub A, Salman S, Khurd A, Der Kalcustian VM (1987): Juvenile hyaline fibromatosis: Two new patients and review of the literature. Am J Med Genet 26:123-131.
6. Gilaberte Y, Gonzalez-Mediero I, Lopez Barrantes V, Zambrano A (1993): Juvenile hyaline fibromatosis with skull-encephalic anomalies: A case report and review of the literature. Dermatol 187(2):144-148.
7. Gilchrest BA (1981): Premature aging syndromes affecting the skin. Birth Defects: OAS/XVII(2):227-241.
8. Gilkes JJH, Sharvill DE, Wells RS (1974): The premature aging syndromes: Report of eight cases and description of a new entity named metageria. Br J Dermatol 91:243-262.
9. Gillar PJ, Kaye CI, McCourt JW (1991): Progressive early dermatologic changes in Hutchinson-Gilford Progeria syndrome. Pediatr Dermatol 8(3):199-206.
10. Greally JM, Boone LY, Lenkey SG, Wenger SL, Steele MW (1992): Acrometageria: A spectrum of "premature aging" syndromes. Am J Med Genet 44:334-339.
11. Hagadorn JI, Wilson WG, Hogge WA, Callicott JH, Beale EF (1990): Neonatal progeroid syndrome: More than one disease?. Am J Med Genet 35:91-94.
12. Ishikawa H, Mori S (1973): Systemic hyalinosis or fibromatosis hyalinica multiplex juvenilis as a congenital syndrome. Acta Dermatovenerol 53:185-191.
13. Kan A E, Rogers M (1989): Juvenile hyaline fibromatosis: An expanded clinicopathologic spectrum. Pediatr Dermatol 6(2):68-75.
14. Kitano Y, Horiki M, Aoki T, Sagami S (1972): Two cases of juvenile hyaline fibromatosis: Some histological, EM and tissue culture observations. Arch Dermatol 16:877-883.
15. LeMerrer M, Guillot M, Briard M-L, Maroteaux P (1991): Lethal progeroid syndrome with osteolysis: Case report. Annales de Genetiq 34(2):82-84.
16. Mulvihill JJ, Smith DW (1975): Another disorder with prenatal shortness of stature and prenatal aging. Birth Defects XI(2):368-371.
17. Nance MA, Berry SA (1992): Cockayne syndrome: Review of 140 cases. Am J Med Genet 42(1):68-84.
18. Petty EM, Laxova R, Wiedemann H-R (1990): Previously unrecognized congenital progeroid disorder. Am J Med Genet 35:383-387.
19. Remberger K, Krieg T, Kunze D, Weinmann H-M, Hubner G (1985): Fibromatosis hyalinica multoplex (juvenile hyaline fibromatosis). Cancer 56:614-624.
20. Schrander-Stumpel C, Spaepen A, Fryns J-P, Dumon J (1992) A severe case of mandibuloacral dysplasia in a girl. Am J Med Genet 43:877-881.
21. Sensenbrenner JA, Fiorelle G (1971): New syndrome manifested by mandibular hypoplasia, acroosteolysis, stiff joints and cutaneous atrophy (mandibuloacral dysplasia) in two unrelated boys. Birth Defects: OAS VII(7):294.
22. Sweeney KJ, Weiss AS (1992): Hyaluronic acid in progeria and the aged phenotype? Gerontology 38:139-152.
23. Wang N-S, Knaack J (1982): Fibromatosis hyalinica multiplex juvenilis. Ultrastructural Pathol 3:153-160.
24. Wiedemann HR (1979): An unidentified neonatal progeroid syndrome: Follow up report. Eur J Pediatr 130:65-70.
25. Wollina U, Reuter A, Schaarschmidt H, Muller E, Maak B, Schmidt U (1992): Hutchinson-Gilford syndrome. Hautarzt 43:453-457.
26. Woyke S, Domagala W, Olszewski W (1970): Ultrastructure of a fibromatosis hyalinica multiplex juvenilis. Cancer 26:1157-1168.
27. Young LW, Radebaugh JF, Rubin B (1971): New syndrome manifested by mandibular hypoplasia, acroosteolysis, stiff joints and cutaneous atrophy (mandibuloacral dysplasia) in two unrelated boys. Birth Defects: OAS VII(7):291-297.