Results 31 to 40 of about 2,781,607 (301)

CONGENITAL ANOMALIES OF THE UPPER LIMBS IN A UNIVERSITY CENTER: A CROSS-SECTIONAL STUDY [PDF]

Acta Ortopédica Brasileira
Objective: To identify the prevalence and characteristics of CAULs treated at a university center, aiming to improve epidemiological understanding and management of these conditions.
Danilo José Leite Gomes, Rodrigo Guerra Sabongi, Vinicius Ynoe de Moraes, Luis Renato Nakachima, João Carlos Belloti, Flavio Faloppa   +5 more
doaj   +1 more source

Coping with Congenital Hand Differences [PDF]

, 2015
Background: Although functional outcomes following reconstruction for congenital hand differences are frequently described, much less is known regarding children\u27s ability to cope with the psychosocial effects of these conditions.
Chung, K. C., Chin, A. Y. T., Carlozzi, N., Nellans, K. W., Franzblau, L. E., Waljee, J. F.   +5 more
core   +1 more source

Klippel–Feil Syndrome with Sprengel Deformity and Extensive Upper Extremity Deformity: A Case Report and Literature Review

Case Reports in Orthopedics, 2018
Introduction. Klippel–Feil syndrome (KFS) is a congenital anomaly resulting from fusion of cervical vertebral bodies secondary to the dysregulation of signaling pathways during somite development.
John W. Stelzer, Miguel A. Flores, Waleed Mohammad, Nathan Esplin, Jonathan J. Mayl, Christopher Wasyliw   +5 more
doaj   +1 more source

A Case Report of Primary Hypertrophic Osteoarthropathy

罕见病研究
Primary hypertrophic osteoarthropathy(PHO) is a rare disease also known as pachydermoperiostosis. We reported a painless case whose diagnosis was confirmed by genetic test. A 24-year-old male presented a series of symptoms that first began at 14.
ZHAO Zongxuan, SUN Liying, CHEN Jia, WANG Yanyuan, CHEN Dan, ZUO Qingyao, DENG Wei, TIAN Wen   +7 more
doaj   +1 more source

Amniotic band syndrome [PDF]

Perspectives In Medical Research, 2018
Amniotic band syndrome (ABS) is a well-described clinical entity, which includes several congenital deformities. Misdiagnosis is common for this entity. Incidence being 1 in 12000 births. Hand malformations and limb defects are frequent ,constriction
K S K Divya1 ,Vivekanand Achanta2
doaj  

Clinical and genetic features, surgical management, and longitudinal follow-up in two children with progressive osseous heteroplasia

Frontiers in Genetics
BackgroundProgressive osseous heteroplasia (POH) is an ultrarare disorder characterized by heterotopic ossification that progresses from the skin and subcutaneous tissues into deeper connective tissues.
Yuehan Yin, Binshan Zhao, Liying Sun, Wenyao Zhong, Dan Chen, Xiuli Zhao, Wen Tian   +6 more
doaj   +1 more source

Congenital Deformities of Hand. [PDF]

JAMA: The Journal of the American Medical Association, 1899
Philadelphia,Pa., March 21, 1899. To the Editor: —Referring to Dr. F. R. Sherwood's very meritorious article in theJournalof March 11, on the above subject, I am constrained to contribute this brief record of an observation, made en passant as it were, which may possess some interest for the doctor, and for some other readers.
openaire   +1 more source

Congenital Malformation of the Hand

, 1999
Congenital malformation of the hand and forearm are rare. Between 2% and 4% of all children are born with a more or less distinct malformation of the hand.
Jörg Grünert
core   +1 more source

Congenital hand anomalies: etiology, classification, and treatment

, 2014
Congenital hand anomalies have a wide range of presentations and functional consequences. Understanding and treatment of these deformities require an understanding of embryology of upper-extremity development. In this report, common anomalies of the hand
Gishen, Kriya, Askari, Morad
core   +1 more source

Delayed presentation of ulnar drift of the hand; A case report

JPRAS Open
Purpose of paper: To present a case of delayed presentation of congenital ulnar drift of the hand. Background: Congenital ulnar drift, frequently known as windblown hand, represents ulnar deviation of fingers with or without other malformations that are ...
Aeshah Abdulrahman Aljayban, Bassmh A. Al-Dhafer   +1 more
doaj   +1 more source