Additional metatarsal bones in Apert's syndrome

Foot

Volumn 6, Issue 1, 1996, Pages 37-38

  Anderson, P J ^a   Smith, P J ^a   Jones, B M ^a   Hayward, R D ^a  

^a GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; ARTICLE; CASE REPORT; CHILD; CRANIOFACIAL MORPHOLOGY; FEMALE; FOOT; FUNCTIONAL ANATOMY; HUMAN; INFANT; METATARSAL BONE; PRIORITY JOURNAL; RADIODIAGNOSIS; SYNDACTYLY;

EID: 0029867847     PISSN: 09582592     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0958-2592(96)90059-0     Document Type: Article

References (6)

1. Kaplan C K. Clinical assesment and multispeciality management of Apert syndrome. In: Upton J, Zucker R M, eds. Apert Syndrome. Clinics in Plastic Surgery, vol 18. Philadelphia: Saunders, 1991: 217-225.
2. Wilkie AOM, Slaney S F, Oldridge M et al. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genetics 1995; 9: 165-171.
3. Hoover G H, Flatt A E, Weiss M W. The hand and Apert's syndrome. J Bone Joint Surg [Am] 1970; 52A: 878-895.
4. Schauerte E W, St-Aubin P M. Progressive synostosis in Apert syndrome (acrocephalosyndactyly), with a description of roentgenographic changes of the feet. Am J Roentgenol 1966; 97: 67-73.
5. Pfeiffer R D. Associated deformities of the head and hands. Birth Defects 1969; 5: 18-34.
6. Mah J, Kasser J, Upton J. The Foot in Apert syndrome. In: Upton J, Zucker R M, eds. Apert Syndrome. Clinics in Plastic Surgery vol 18. Philadelphia: Saunders, 1991: 391-397.