Association of intermediate osteopetrosis with poikiloderma

Journal of Bone and Mineral Research

Volumn 14, Issue 5, 1999, Pages 834-836

  Migliaccio, S ^a   Luciani, M ^b   Taranta, A ^a   De Rossi, G ^b   Minisola, S ^a   El Hachem, M ^b   Bosman, C ^c   De Felice, L ^a   Boldrini, R ^b   Corsi, A ^d   Bianco, P ^d   Teti, Anna ^d,e  

^a SAPIENZA UNIVERSITY OF ROME   (Italy)

^b BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

^d UNIVERSITY OF L'AQUILA   (Italy)

^e NONE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALBERS SCHOENBERG DISEASE; ARTICLE; CASE REPORT; CHILD; DISEASE ASSOCIATION; FEMALE; HUMAN; HYPERPIGMENTATION; OSTEOSCLEROSIS; POIKILODERMA; SKIN DISEASE;

CHILD; FEMALE; HUMANS; OSTEOPETROSIS; ROTHMUND-THOMSON SYNDROME;

EID: 0032897309     PISSN: 08840431     EISSN: None     Source Type: Journal    
DOI: 10.1359/jbmr.1999.14.5.834     Document Type: Article

References (4)

1. Vennos EM, Collins M, James WD 1992 Rothmund-Thompson syndrome: A review of the world literature. Am Acad Dermatol 27:750-762.
2. Nii A, Steingrimsson E, Copeland NG, Jenkins NA, Wad JM 1995 Mild osteopetrosis in the microphtalmia-oak ridge mouse: A model for intermediate autosomal recessive osteopetrosis in humans. Am J Pathol 147:1871-1882.
3. Kahele SG, Burns JA, Aylsworth AS 1984 A mild autosomal recessive form of osteopetrosis. Am J Med Genet 17:451-464.
4. Beard CJ, Key L, Newburger PE, Ezekowitz AB, Arceci R, Miller B, Proto P, Ryan T, Anast C, Simons ER 1986 Neutrophil defect associated with malignant infan osteopetrosis. J Lab Clin Med 108:498-505.