Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Lobster claw hand"'
Autor:
Deepak eSharma, Chetan eKumar, Sanjay eBhalerao, Aakash ePandita, Sweta eShastri, Pradeep eSharma
Publikováno v:
Frontiers in Pediatrics, Vol 3 (2015)
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome (EEC) syndrome is a rare genetic disorder with an incidence of around 1:90,000 live births. It is known with various names which includes split hand–split foot–ectodermal dysplasia
Externí odkaz:
https://doaj.org/article/23fb2c4e071f4c3c89135ae83e6a7a81
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 12, Pp AD06-AD08 (2014)
An asymptomatic atypical U shaped cleft hand has been found in a 21-year-old lady attending OPD. On digital skiagram it was found that central digits were absent with remnants of bases of the metacarpals, which have fused with the carpal bones. More
Externí odkaz:
https://doaj.org/article/11604310f6e84fddbe0c40b8f99bfbf0
Autor:
Anupam Das, Rajesh Kumar Mandal
Publikováno v:
Indian Dermatology Online Journal, Vol 12, Iss 6, Pp 944-945 (2021)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb232b416cfaf3099e7b9e3e33440cc7
http://www.idoj.in/article.asp?issn=2229-5178
http://www.idoj.in/article.asp?issn=2229-5178
Autor:
Sahana M Srinivas, Ravi Hiremagalore
Publikováno v:
Indian Journal of Dermatology, Vol 60, Iss 1, Pp 106-106 (2015)
Focal dermal hypoplasia (Goltz syndrome) is a rare genetic multisystem disorder primarily involving the skin, skeletal system, eyes, and face. We report the case of an eight-month-old female child who presented with multiple hypopigmented atrophic ma
Externí odkaz:
https://doaj.org/article/4b4b2475ff4f46e0bc88d61472a92d94
Publikováno v:
Journal of Mahatma Gandhi Institute of Medical Sciences, Vol 21, Iss 1, Pp 72-74 (2016)
Split-hand/split-foot malformation (SHFM), a congenital limb malformation, occurs due to the absence of the central rays of autopod that results in a deep median cleft of the hand and/or foot. It is also known as ectrodactyly or lobster claw hand. Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7264226464173144efc440841c2bfacf
http://www.jmgims.co.in/article.asp?issn=0971-9903
http://www.jmgims.co.in/article.asp?issn=0971-9903
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 12, Pp AD06-AD08 (2014)
An asymptomatic atypical U shaped cleft hand has been found in a 21-year-old lady attending OPD. On digital skiagram it was found that central digits were absent with remnants of bases of the metacarpals, which have fused with the carpal bones. Moreo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e9d28d52f84f9e6bb5d62126023bfb2
https://europepmc.org/articles/PMC4316240/
https://europepmc.org/articles/PMC4316240/
Publikováno v:
International Journal of Anatomy and Research. 3:845-847
Address for Correspondence: Dr. Subhra Mandal, M.B.B.S., M.D. (Anatomy), Associate Professor, Dept. of Anatomy, Medical College, Kolkata, West Bengal, India. Contact No.: +919477458100 E-Mail: drsuvramandal@gmail.com Access this Article online Quick
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::143d47f133fa00d99e3ed2046a5f8b03
https://doi.org/10.16965/ijar.2015.101
https://doi.org/10.16965/ijar.2015.101
Publikováno v:
International Journal of Contemporary Pediatrics. :1121-1122
Ectrodactyly also called as split hand or foot malformation (SHFM).Congenital absence of all or part of one or more fingers or toes is defined as Ectrodactyly. Irregular pattern of inheritance exists for ectrodactyly, may be autosomal dominant, autos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0ae6c1d77ca225e49271dd015cb24c6
https://doi.org/10.18203/2349-3291.ijcp20162406
https://doi.org/10.18203/2349-3291.ijcp20162406
Publikováno v:
Indian Journal of Dermatology, Venereology and Leprology, Vol 71, Iss 4, Pp 279-281 (2005)
A 7-year-old girl born of non-consanguineous marriage was evaluated for facial dysmorphism. She had multiple skeletal anomalies like hypoplasia of the right mandible, narrow nasal bridge with broad tip and unilateral notching of the right ala nasi, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b8d8856b0838c3baf043a7055e82eea
http://www.ijdvl.com/article.asp?issn=0378-6323
http://www.ijdvl.com/article.asp?issn=0378-6323
Publikováno v:
Saudi Journal of Sports Medicine. 17:53
Congenital longitudinal tibial hemimelia is a rare disorder of lower limbs. This disorder is usually associated with skeletal and extraskeletal congenital malformation. The treatment depends on the type of tibial hemimelia. Multiple reconstructive su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6f1a56ceb5afa33129ae942a17f25a7
https://doi.org/10.4103/1319-6308.197472
https://doi.org/10.4103/1319-6308.197472