SE-ATLAS

Dysostose oculo-maxillo-faciale Syndrome de Jackson-Weiss Craniosynostose type Boston Syndrome oro-facio-digital type 14 Syndrome de Goodman Dysostose craniofaciale Syndrome oro-facio-digital type 12 Syndrome oro-facio-digital type 13 Syndrome de Lambert Syndrome de Curry-Jones Syndrome de cutis gyrata-acanthosis nigricans-craniosynostose Encéphalocèle occipitale Craniosynostose sagittale non syndromique Syndrome de Muenke Encéphalocèle basale Syndrome de Saethre-Chotzen Plagiocéphalie isolée Craniosynostose bicoronale non syndromique Syndrome C Syndrome de Stickler type 1 Encéphalocèle pariétale Syndrome de Stickler type 2 Syndrome létal d'encéphalocèle occipital-dysplasie squelettique Syndrome de dysostose mandibulo-faciale-macroblépharon-macrostomie Dysplasie frontonasale acromélique Syndrome de Pierre Robin-déficience intellectuelle-brachydactylie Syndrome de trigonocéphalie-anomalies des extrémités Syndrome de dysplasie frontonasale-alopécie-anomalies génitales Syndrome de Pierre Robin-contractures-retard de développement Craniosynostose métopique non syndromique Crâne en trèfle isolé Frontorhinie Syndrome de délétion 22q11.2 Syndrome de Pierre Robin associée à une collagénopathie Syndrome de Stickler Syndrome de craniosynostose-hydrocéphalie-malformation d'Arnold-Chiari type I-synostose radio-ulnaire Maladie rare avec syndrome de Pierre Robin Spectre oculo-auriculo-vertébral Syndrome de crâne en trèfle-anomalies congénitales multiples Syndrome de craniosynostose-calcifications intracrâniennes Syndrome de Treacher-Collins Syndrome de dysplasie frontonasale-microphtalmie sévère-fente faciale sévère Syndrome de crâne en trèfle-dysplasie asphyxiante du thorax Craniosynostose syndromique Encéphalocèle frontale Auriculocondylar syndrome Acrodysostosis Dobrow syndrome Orofaciodigital syndrome type 2 Orofaciodigital syndrome type 4 Familial scaphocephaly syndrome Orofaciodigital syndrome type 11 Orofaciodigital syndrome type 9 Submucosal cleft palate Non-syndromic bilambdoid and sagittal craniosynostosis Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome Craniofrontonasal dysplasia-Poland anomaly syndrome Craniomicromelic syndrome Nager syndrome Craniotelencephalic dysplasia Mandibulofacial dysostosis Craniosynostosis-cataract syndrome Otomandibular dysplasia associated with monogenic syndromes Trigonocephaly-short stature-developmental delay syndrome Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome Pierre Robin syndrome associated with a chromosomal anomaly SCARF syndrome Pierre Robin syndrome associated with branchial archs anomalies Pierre Robin syndrome associated with bone disease TARP syndrome Teratogenic Pierre Robin syndrome Crouzon syndrome-acanthosis nigricans syndrome X-linked intellectual disability-plagiocephaly syndrome BOR syndrome Goldenhar syndrome Isolated cleft lip Weiss-Kruszka Syndrome Shprintzen-Goldberg syndrome Bifid uvula Orofaciodigital syndrome type 1 Orofaciodigital syndrome type 6 Pseudoaminopterin syndrome Orofaciodigital syndrome Osteosclerosis-developmental delay-craniosynostosis syndrome Crouzon syndrome Isolated encephalocele Cranioectodermal dysplasia SPECC1L-related hypertelorism syndrome SIX2-related frontonasal dysplasia Craniosynostosis, Philadelphia type Frontonasal dysplasia Otomandibular dysplasia FGFR2-related bent bone dysplasia Frontofacionasal dysplasia Cardiocranial syndrome, Pfeiffer type Nasal encephalocele Hunter-McAlpine syndrome Oculoauriculofrontonasal syndrome Acrodysostosis with multiple hormone resistance Oral-facial-digital syndrome with short stature and brachymesophalangy Townes-Brocks syndrome Orofaciodigital syndrome type 5 Autosomal recessive Stickler syndrome Non-syndromic craniosynostosis Cleft lip/palate Cleft hard palate Craniofaciofrontodigital syndrome Orofaciodigital syndrome type 10 Pfeiffer syndrome Baller-Gerold syndrome Isolated Pierre Robin syndrome Isolated oxycephaly Teebi-Shaltout syndrome Cleft palate Craniofrontonasal dysplasia Pfeiffer syndrome type 2 Pfeiffer syndrome type 1 Pfeiffer syndrome type 3 Otomandibular syndrome Antley-Bixler syndrome Apert syndrome Mandibulofacial dysostosis with alopecia Craniosynostosis, Herrmann-Opitz type Lowry-MacLean syndrome Holoprosencephaly-craniosynostosis syndrome Acrocephalopolydactyly Summitt syndrome Acrocephalosyndactyly Cleft velum Orofaciodigital syndrome type 3 Familial lambdoid synostosis Orofaciodigital syndrome type 8 Pai syndrome Craniosynostosis-anal anomalies-porokeratosis syndrome Familial osteodysplasia, Anderson type Carpenter syndrome Cantú syndrome Craniosynostosis-dental anomalies Oculoauriculovertebral spectrum with radial defects Craniosynostosis-fibular aplasia syndrome