Y a-t-il des traitements expérimentaux disponibles ?
Des recherches sont en cours, mais aucun traitement expérimental n'est encore validé.
Traitements expérimentauxRecherche
#5
Les soins de soutien sont-ils importants ?
Oui, les soins de soutien sont cruciaux pour améliorer la qualité de vie des patients.
Soins de soutienQualité de vie
Complications
5
#1
Quelles sont les complications possibles de la dysplasie thanatophore ?
Les complications incluent des problèmes respiratoires, des infections et des déformations osseuses.
ComplicationsInfections
#2
Les patients peuvent-ils avoir des problèmes cardiaques ?
Des problèmes cardiaques ne sont pas typiques, mais des évaluations sont recommandées.
Problèmes cardiaquesÉvaluations
#3
Comment les complications affectent-elles la survie ?
Les complications respiratoires sévères peuvent réduire l'espérance de vie des patients.
SurvieEspérance de vie
#4
Les déformations osseuses peuvent-elles s'aggraver ?
Oui, sans intervention, les déformations peuvent s'aggraver avec la croissance.
Déformations osseusesCroissance
#5
Y a-t-il un risque accru d'infections ?
Oui, les patients peuvent être plus susceptibles aux infections en raison de leur condition.
InfectionsSusceptibilité
Facteurs de risque
5
#1
Quels sont les facteurs de risque de la dysplasie thanatophore ?
Les facteurs incluent des antécédents familiaux et des mutations génétiques spécifiques.
Facteurs de risqueAntécédents familiaux
#2
L'âge des parents influence-t-il le risque ?
Oui, l'âge avancé des parents peut augmenter le risque de malformations congénitales.
Âge des parentsMalformations congénitales
#3
Y a-t-il des liens avec d'autres conditions génétiques ?
Certaines conditions génétiques peuvent coexister, mais la dysplasie thanatophore est spécifique.
Conditions génétiquesDysplasie
#4
Les antécédents de fausses couches sont-ils un facteur ?
Des antécédents de fausses couches peuvent indiquer un risque accru de malformations.
Fausses couchesMalformations
#5
Les facteurs environnementaux jouent-ils un rôle ?
Actuellement, aucun facteur environnemental n'est clairement associé à la dysplasie thanatophore.
Facteurs environnementauxDysplasie
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"@type": "Question",
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"@type": "Question",
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"position": 9,
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"position": 12,
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"position": 16,
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"@type": "Answer",
"text": "Il n'existe pas de traitement curatif, mais des soins palliatifs peuvent être offerts."
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},
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"name": "La chirurgie est-elle une option pour ces patients ?",
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"@type": "Answer",
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"name": "Y a-t-il des liens avec d'autres conditions génétiques ?",
"position": 28,
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"@type": "Question",
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"@type": "Question",
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"position": 30,
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Section of Neonatal-Perinatal Medicine, Department of Pediatrics, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, OH, USA.
Section of Neonatal-Perinatal Medicine, Department of Pediatrics, Drexel University College of Medicine, St. Christopher's Hospital for Children, Philadelphia, PA, USA. bhandari-vineet@cooperhealth.edu.
Neonatology Research Laboratory, Education and Research Building, Cooper University Hospital, (Room #206), Camden, NJ, USA. bhandari-vineet@cooperhealth.edu.
Department of Pediatrics, Section of Pulmonary and Sleep Medicine, University of Colorado School of Medicine, 13123 East 16th Avenue Box B-395, Aurora, CO 80045, USA.
Department of Radiology, University of Iowa Hospitals and Clinics, Iowa City, IA, USA. atsuhiko.handa@childrens.harvard.edu.
Department of Radiology, Boston Children's Hospital and Harvard Medical School, 300 Longwood Ave, Boston, MA, 02115, USA. atsuhiko.handa@childrens.harvard.edu.
Department of Orthopaedic Surgery, Department of Human Genetics and Department of Obstetrics and Gynecology, David Geffen School of Medicine at UCLA, University of California, Los Angeles, Los Angeles, CA 90095, USA.
We report the rare case of a 3-year-old male patient with thanatophoric dwarfism, a fatal skeletal dysplasia that arises from an autosomal dominant mutation in the fibroblast growth factor receptor 3 ...
We advocate for the close monitoring of disease progression by the orthopaedic surgery team and offer a potential surgical intervention that may help prevent cardiorespiratory demise....
Thanatophoric dysplasia is a rare, fatal, and sporadic form of skeletal dysplasia caused by a mutation in fibroblast growth factor receptor 3 (FGFR3). It is characterized by a conical thorax, platyspo...
The authors reported a case of thanatophoric dysplasia on USG in a 19 year old young consanguineous female in her second trimester of pregnancy. Ultrasound examination showed a clover leaf-shaped skul...
Lung hypoplasia, polyhydramnios, and hydrops in affected individuals lead to a poor prognosis. Hence, timely intervention should be done to avoid a poor prognosis. However, a mix of sonographic, genet...
The authors reported this case due to the rarity of this condition and the need for a systematic and multidisciplinary approach....
Mutation analysis is used to provide confirmation of a clinical and radiological diagnosis of Thanatophoric dysplasia types I and II (TDI & II). We developed a single multiplexed PCR and a single nucl...
The World Health Organization's definition of oral epithelial dysplasia includes differentiated dysplasia, which is defined by purely architectural abnormalities of oral mucosa without cytological cha...
Cytoarchitectural criteria and expression patterns of keratin 13/17 and ki67 were studied in oral biopsies clinically diagnosed with leukoplakia. Biopsies were assessed for dysplasia and its grade. Av...
We included 159 biopsies from 112 patients (33% differentiated dysplasia; 27% keratosis without dysplasia; oral epithelial dysplasia with atypia of mild, moderate and severe degree including invasive ...
Keratin 17 but not oral brush cytology can help identify patients with differentiated dysplasia with higher risk for malignant transformation....
Fibrocartilaginous dysplasia (FCD) is a subvariant of fibrous dysplasia (FD). This study aims to retrospectively elucidate the clinicopathological and separate genetic features of the cartilaginous an...
In total, 24 patients (14 men and 10 women) with FCD were included in our cohort. The diagnosis was confirmed morphologically and immunohistochemically, and genetic features were determined via Sanger...
Five patients were polyostotic, and 19 were monostotic, predominantly concerning the femur. Radiography revealed a well-demarcated ground glass appearance with ring-like or scattered calcification. Hi...
FCD encompasses areas of conventional FD with additional cartilage. Importantly, the presence or absence of mutations in the...
Fibrous dysplasia is a sporadically occurring benign skeletal disease characterized by the replacement of normal bone tissue with excessively proliferating cellular fibrous tissue. It can occur in a m...
Hip dysplasia is one of the most common malformations in childhood and has a significant impact on the further life of those affected. A distinction must be made between congenital and the much rarer ...
The paper gives an overview of current radiological possibilities of diagnosis with focus on congenital hip dysplasia supplemented by insights into therapeutic options....
Basic and review papers were analyzed....
Clinical examination of the newborn has low sensitivity and specificity in the diagnosis of hip dysplasia. The introduction of Graf ultrasound screening has significantly improved the early detection ...
Early detection of hip dysplasia is critical to the course of treatment. The right choice of examination method and correct performance are essential for further treatment....
Oral epithelial dysplasia associated with high-risk HPV infection has received different names since its initial description, such as oral Bowenoid lesions, HPV-associated intraepithelial neoplasia, a...
Developmental dysplasia of the hip (DDH) and trochlear dysplasia (TD) are distinct pathologies with several important features in common. In addition to shared risk factors, both forms of dysplasia ca...
To evaluate for an association between hip dysplasia and TD in skeletally mature patients with symptomatic hip dysplasia....
Cross-sectional study; Level of evidence, 3....
A total of 48 patients with DDH who underwent periacetabular osteotomy were compared with 48 sex-matched patients who underwent hip arthroscopy for femoroacetabular impingement (FAI) between July 2014...
Patients with DDH demonstrated a reduced trochlear depth compared with patients with FAI (3.6 vs 4.6 mm;...
Patients with DDH had reduced trochlear depth compared with patients with FAI, demonstrating a higher incidence of dysplastic trochlear features that may predispose patients to patellofemoral joint di...
Skeletal dysplasias (SDs) are a diverse group of genetic disorders. Diagnosis can be difficult as many are rare and with varied presentations, but with knowledge of the most common SDs presenting pren...