Results 21 to 30 of about 32,192 (76)

Klippel–Feil syndrome with inherited coagulopathy: A rare case report

, 2017
Klippel–Feil syndrome is a rare disease known to be associated with many musculoskeletal as well as somatic diseases. Thromboembolism is one of the complications, which although rarely described earlier with this syndrome, can be life-threatening ...
Sameer Bansal, Jyotsna M Joshi, Ketaki Utpat   +2 more
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Mutation in gene causes a recessive Klippel-Feil syndrome subtype [PDF]

, 2013
Background: Klippel-Feil syndrome (KFS) is characterized by the developmental failure of the cervical spine and has two dominantly inherited subtypes.
Balaban, Hatice, Burak Kazanci, Ugur Kartal, Ozum, Unal, Yuksel, Sirin, Ahmet Ozturk, Bayraklı, Fatih, Kazanci, Burak, Mahmut Sagiroglu, Bayrakli, Fatih, Sagiroglu, Mahmut Samil, Ozturk, Ahmet, Kars, Hamit, Fatih Bayrakli, Hatice Balaban, Bekir Erguner, Sirin Yuksel, Hamit Kars, Yakicier, Cengiz, Sagiroglu, Mahmut, Bulent Guclu, Cengiz Yakicier, Kars, Hamit Zafer, Erguner, Bekir, Ozturk, Ahmet Rasit, Unal Ozum, Kartal, Ugur, Guclu, Bulent   +27 more
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Congenital Cervical Vertebrae Clefts In Klippel-Feil Syndrome

Congenital Cervical Vertebrae Clefts In Klippel-Feil ...
Blanco Pérez, Esther, Sánchez Jurado, Raúl, Mata-Escolano, Federico, Aparicio, Luis, Sanchis-Gimeno, Juan A., Llidó-Torrent, Susana   +5 more
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Diagnosis and management of klippel–feil syndrome

, 2018
Klippel–Feil syndrome (KFS) is a congenital malformation of the cervical vertebrae, with limited treatment options. Short neck, limitation of neck motion, and low occipital hairline form the classical triad of KFS.
Ashok Alapati, Susheel, Kurian Zachariah, Reddy Ravikanth   +3 more
core   +1 more source

Severe Klippel-Feil syndrome with Mondini malformation of inner ear [PDF]

, 2014
Klippel-Feil syndrome is defined as the fusion of cervical vertebra with associated congenital anomalies but was rarely reported to be associated with Mondini Malformation.
Aqeel Abdullah Alaqeel
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Klippel-Feil syndrome associated with persistent trigeminal artery [PDF]

, 2004
Study Design. In the present report, radiologic findings of the patient with the Klippel-Feil syndrome associated with persistent trigeminal artery are reviewed.
Kalkan, E, Paksoy, Y, Seker, M
core   +1 more source

Case Report KLIPPEL-FEIL SYNDROME, A RARE PRESENTATION - CASE REPORT

, 2020
Klippel-feil syndrome is a bone disorder characterized by the abnormal joining (fusion) of two or more spinal bones in the neck (cervical vertebrae), which is present from birth.
Ravi Chander B, Neha Srivasthava, Krapa Vijay, Revanasiddappa Bhosgi, Ravi Kumar   +4 more
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Autosomal dominant Klippel-Feil anomaly with cleft palate

, 1998
Klippel-Feil anomaly is characterized by the fusion of two or more cervical vertebrae. Most cases are sporadic but dominant and recessive inheritance are well described. Associated anomalies such as a cleft palate are common.
Sheffield, L., Haan, E., Thompson, E.
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A giant hypertrophy of C5 spinous process in Klippel-Feil syndrome

, 2015
Konjenital servikal omurga anomalileri sık olarak alt ve üst servikal bölgede görülebilir.Ancak, tek taraflı lamina ve spinöz proçes hipertrofisi oldukça nadirdir. Literatür taramamızdayayınlamış sadece 4 vaka bulabildik.
MESUT METE, Ahmet Şükrü UMUR, Ülkün Ünlü ÜNSAL, Yusuf Kurtuluş DURANSOY, Mehmet SELÇUKİ   +4 more
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Síndrome de Klippel Feil actualización de tratamiento en pacientes pediátricos. Revisión bibliográfica. [PDF]

, 2022
El trabajo tiene como título “Síndrome de Klippel Feil actualización de tratamiento en pacientes pediátricos. Revisión bibliográfica”, donde el objetivo principal es analizar el síndrome de Klippel Feil para la actualización de tratamiento en pacientes ...
Idrovo Espinoza, María Augusta
core   +1 more source