Results 81 to 90 of about 961 (204)

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11. [PDF]

, 1996
A contiguous gene syndrome due to deletions of the proximal short arm of chromosome 11 is described in eight patients belonging to four families. The main clinical features are multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and ...
Bartsch, Oliver, Wuyts, Wim, Van Hul, Wim, Hecht, Jacqueline T., Meinecke, Peter, Hogue, Debra, Werner, Walter, Zabel, Bernard, Hinkel, Georg K., Powell, Cynthia M., Shaffer, Lisa G., Willems, Patrick J.   +11 more
core   +2 more sources

Acrocephalosyndactyly Syndrome: A Rare Case Report

, 2021
Satya Ranjan Misra
openalex   +2 more sources

Tarsal coalition (rigid flatfoot) [PDF]

, 2012
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and therapeutics of tarsal ...
Burroughs, Kevin, Vasser, Elizabeth C.
core  

Acne-Associated Syndromes [PDF]

, 2017
Introduction: Acne, a chronic inflammatory disorder of pilosebaceous unit, is characterized by comedones, pustules, papules, nodules, cysts, and scars. It affects nearly 85% of adolescents.
Emiroglu, Nazan
core   +2 more sources

Apert syndrome

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2010
Apert syndrome (acrocephalosyndactyly) is a rare developmental malformation characterized by craniosynostosis, mid-face hypoplasia, symmetrical syndactyly of hands and feet. The prodromal characteristics for the typical cranio-facial appearance are early
Premalatha, Kannan V, Madhu
doaj  

Apert Syndrome: New Treatment and a Perspective for the Future [PDF]

, 2015
Treatment the Apert Syndrome is unique, therefore, divergences exist in the priority of the procedures performed by each team. The Apert Syndrome occurs in approximately 1/65,000 births and accounts for 4.5% of all craniosynostosis. Some changes in Apert
Barbosa do Nascimento, Vânia, Batista Pereira, Janaina, Braga, Hiroe Alencar, Caldas Lins, Hellen Lúcia, de Matos Cassiano, Cícera Janielly, Gonçalves Leite, Bruno, Gonçalves Pinheiro, Patrícia, Rolim Neto, Modesto Leite, Silva Damasceno, Kécia, Tavares Filgueiras, Ana Beatriz   +9 more
core   +1 more source

Meinhard Robinow: An appreciation [PDF]

, 1995
No Abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/38264/1/1320590103_ftp ...
Lenz, McKusick, Robinow, Sobel
core   +1 more source

Maxillary Changes Following Facial Bipartition – A Three-Dimensional Quantification [PDF]

, 2021
INTRODUCTION: Children with Apert syndrome have hypertelorism and midfacial hypoplasia, which can be treated with facial bipartition (FB), often aided by rigid external distraction.
Dunaway, DJ, Evans, RD, Gill, DS, O'Sullivan, E, Ong, J, Rickart, AJ, Schievano, S, van de Lande, LS   +7 more
core  

Apert's syndrome [PDF]

, 2004
Apert's syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, mid-facial malformations and symmetrical syndactyly.
Mukhopadhyay Amiya Kumar , Mukherjee Debjani
core  

A rare case of neonatal Apert syndrome [PDF]

Apert syndrome is a rare Type I acrocephalosyndactyly syndrome. It is a congenital disorder characterized by premature fusionof cranial sutures (craniosynostosis), malformation of skull, hands, face, and feet.
Ahmed, S K Nazeer, Kumar, T Ravi
core   +1 more source