Zobrazeno 1 - 10
of 781
pro vyhledávání: '"Macrodactyly"'
Autor:
Kaja Giżewska-Kacprzak, Maximilian Śliwiński, Karol Nicieja, Lidia Babiak-Choroszczak, Ireneusz Walaszek
Publikováno v:
Children, Vol 11, Iss 7, p 753 (2024)
Macrodactyly is a rare congenital limb difference manifesting as an overgrowth of one or more fingers or toes. The pathological process affects all tissues of the ray in the hand or foot. The enlargement can significantly alter the limb’s appearanc
Externí odkaz:
https://doaj.org/article/229683674dcf4226ad1d49caeda8e3e1
Autor:
Rishabh Pratap, MBBS, Gaurav Raj, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 4, Pp 1613-1616 (2023)
Macrodystrophia lipomatosa is a rare form of nonhereditary congenital localized gigantism involving upper and lower limbs and is characterized by overgrowth of all the mesenchymal elements predominantly fibro-adipose component, in the distribution of
Externí odkaz:
https://doaj.org/article/1726dc2b00fe4b869944a3841474c651
Autor:
Inês Da Mata, António Proença Caetano
Publikováno v:
Journal of the Belgian Society of Radiology, Vol 108, Iss 1, Pp 33-33 (2024)
Macrodactyly, a often congenital anomaly, entails abnormal enlargement of digits, predominantly affecting hands or feet, either in isolation or as part of a syndromic condition. The authors present a case of Macrodystrophia Lipomatosa (ML), a form of
Externí odkaz:
https://doaj.org/article/1f492f0b354f486ab7dec603e1b719cd
Publikováno v:
Malaysian Orthopaedic Journal, Vol 16, Iss 2, Pp 136-139 (2022)
Macrodystrophia Lipomatosa (MDL) of the toe is a rare, congenital, disproportionate overgrowth involving one or more digits in the lower limb. Despite being a benign condition, when left untreated, it may cause physical impairment and interfere with
Externí odkaz:
https://doaj.org/article/65a57a9cd9674855aa267ecd104afa8a
Publikováno v:
JPRAS Open, Vol 31, Iss , Pp 10-21 (2022)
Background: Macrodactyly is a rare congenital disorder of overgrowth affecting the digits of the upper or lower extremity. Mostly, patients are surgically treated during childhood to reduce the digit or to stop growth. There are no standardized guide
Externí odkaz:
https://doaj.org/article/ce689c643c6f4e38ba93192585322d1d
Publikováno v:
Journal of Primary Care Dentistry and Oral Health, Vol 3, Iss 2, Pp 50-53 (2022)
Klippel–Trenaunay syndrome (KTS) is a congenital, uncommon but a well-recognized disorder, characterized by cutaneous hemangiomas, varicosities, and unilateral bone and soft tissue hypertrophy with different localization. Generally diagnosed at bir
Externí odkaz:
https://doaj.org/article/4dda4a5f7202493996cc038907e3c429
Publikováno v:
Pharmacogenomics and Personalized Medicine, Vol Volume 15, Pp 55-64 (2022)
Jian-Feng Li,1 Guang-Lei Tian,2 Hui Pan,3 Wen-Tong Zhang,1 Da-Cun Li,1 Jing-Da Liu,1 Liang Zhao,1 Hai-Lei Li1 1Department of Hand Surgery, Beijing Shunyi District Hospital; Shunyi Teaching Hospital of Capital Medical University, Beijing, 101300, Peop
Externí odkaz:
https://doaj.org/article/d54752053bd14c4fa114b915e3ed0ac7
Autor:
Nicola Blum, Matthew P. Harris
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 2 (2023)
Externí odkaz:
https://doaj.org/article/50595cc393134101a131d779819a254f
Autor:
Roy Waknin, MD, Ashley Lynn Evens, MD, Lee Garritt Phillips, MD, Jennifer Neville Kucera, MD, MS
Publikováno v:
Radiology Case Reports, Vol 17, Iss 3, Pp 638-640 (2022)
Fibrolipomatous hamartoma is a rare benign congenital overgrowth of fibroadipose tissue in the nerve sheath. While usually affecting the median nerve, the digits of the hands and feet are sometimes affected and may result in macrodactyly, which is re
Externí odkaz:
https://doaj.org/article/e4a27bad9221465f8f96493564163b66
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.