Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Rolf, Habenicht"'
Publikováno v:
Handchirurgie · Mikrochirurgie · Plastische Chirurgie. 48:41-47
Hintergrund: Bei der Klinodaktylie handelt es sich um eine angeborene seitliche Abwinklung eines Fingers. Meistens ist der Kleinfinger betroffen. Die typische Deltaphalanx ist dreiecks- oder trapezformig und hat eine Abwinklung des Endgliedes nach ra
Publikováno v:
The Journal of hand surgery. 44(5)
Purpose Congenital palmar nail (distal dorsal dimelia [dDD]) of the hand is a rare malformation most commonly affecting the little finger. The purpose of this report was to review the features and associations of this rare disorder and discuss the su
Autor:
Rolf Habenicht, Silke Lohan, Klaus W. Kjaer, F. Muhammad, Stefan Mundlos, Hugo Abarca-Barriga, Ricarda Flöttmann, Shahid Mahmood Baig, Katta M. Girisha, Eva Klopocki, Malte Spielmann, Wiebke Hülsemann, Sandra C. Doelken, Siddaramappa J. Patil, Muhammad Wajid
Publikováno v:
Clinical Genetics. 86:318-325
Laurin-Sandrow syndrome (LSS) is a rare autosomal dominant disorder characterized by polysyndactyly of hands and/or feet, mirror image duplication of the feet, nasal defects, and loss of identity between fibula and tibia. The genetic basis of LSS is
Publikováno v:
Handchirurgie · Mikrochirurgie · Plastische Chirurgie. 45:265-270
Kindlichen Nervenverletzungen wird gegenuber denen von Erwachsenen eine bessere Regenerationsfahigkeit nach operativer Versorgung zugeschrieben, die Datenlage hierzu ist jedoch begrenzt. Ziel dieser Arbeit ist es, anhand des eigenen Patientengutes so
Publikováno v:
Journal of Plastic, Reconstructive & Aesthetic Surgery. 66:1117-1122
Summary Background In amniotic band syndrome (ABS) constriction rings affecting the limbs are regularly seen at birth. Circular resection and closure with multiple Z-plasties has been described as the treatment of choice. However, direct circular clo
Autor:
Ingo Kurth, Denise Horn, Outi Mäkitie, Eva Klopocki, Regina Célia Mingroni Netto, Anna Rajab, Charlotte W. Ockeloen, Silke Lohan, Hitesh Shah, Renata Soares Thiele de Aguiar, Maja Hempel, Matthew L. Warman, Aleksander Jamsheer, Rolf Habenicht, Karina Lezirovitz, Stylianos E. Antonarakis, Stefan Mundlos, Uppala Radhakrishna, Sandra C. Doelken, Koenraad Devriendt, Mohammed Naveed, Sigmar Stricker, Ulrike Kordaß
Publikováno v:
Journal of Medical Genetics (London)
Journal of Medical Genetics, Vol. 49, No 2 (2012) pp. 119-25
Journal of Medical Genetics, 49, 119-25
Journal of Medical Genetics, 49, 2, pp. 119-25
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Journal of medical genetics
Journal of Medical Genetics, Vol. 49, No 2 (2012) pp. 119-25
Journal of Medical Genetics, 49, 119-25
Journal of Medical Genetics, 49, 2, pp. 119-25
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Journal of medical genetics
BACKGROUND: Split-hand/foot malformation (SHFM)-also known as ectrodactyly-is a congenital disorder characterised by severe malformations of the distal limbs affecting the central rays of hands and/or feet. A distinct entity termed SHFLD presents wit
Publikováno v:
Obere Extremität. 5:151-157
Bei den dislozierten suprakondylaren Humerusfrakturen treten relativ haufig neurovaskulare Begleitschaden und iatrogene Nervenlasionen auf. Traumatische Nervenschadigungen und Durchblutungsstorungen bilden sich ublicherweise nach der Reposition und F
Publikováno v:
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie. 26(2)
Introduction The majority of pediatric phalangeal fractures yield excellent results following conservative or operative treatment. However, a certain subset of fractures is associated with long-term sequelae such as osteonecrosis, physeal growth arre
Autor:
Scott N. Oishi, Charles A. Goldfarb, Samantha L. Piper, Rolf Habenicht, Marybeth Ezaki, Lindley B. Wall
Publikováno v:
The Journal of hand surgery. 40(9)
Purpose To investigate the distinguishing morphological characteristics of children with radial longitudinal deficiency (RLD) in Holt-Oram syndrome (HOS). Methods One hundred fourteen involved extremities in 62 patients with a diagnosis of HOS were i
Publikováno v:
The Journal of hand surgery, European volume. 41(3)
Various surgical techniques are described for separation of syndactylies leading to good results. However, the use of standard techniques is limited in complex syndactylies with extensive bony fusion and tight soft tissues. The aim of this study was