SE-ATLAS

Goldenhar syndrome Pfeiffer syndrome type 1 Pfeiffer syndrome type 3 Pfeiffer syndrome type 2 Crouzon syndrome-acanthosis nigricans syndrome Rare otorhinolaryngologic disease Nager syndrome Isolated encephalocele Autosomal dominant otospondylomegaepiphyseal dysplasia Osteosclerosis-developmental delay-craniosynostosis syndrome Atelosteogenesis type II Saethre-Chotzen syndrome Atelosteogenesis type III Cloverleaf skull-multiple congenital anomalies syndrome Frontonasal dysplasia Holoprosencephaly-craniosynostosis syndrome Isotretinoin syndrome Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome Dobrow syndrome Acrocephalosyndactyly Familial lambdoid synostosis Non-syndromic craniosynostosis Fetal valproate spectrum disorder SCARF syndrome Baller-Gerold syndrome Rare maxillo-facial surgical disease Aminopterin/methotrexate embryofetopathy Syndromic craniosynostosis Indomethacin embryofetopathy Smith-Lemli-Opitz syndrome Intellectual disability-brachydactyly-Pierre Robin syndrome Fetal iodine syndrome Smith-Magenis syndrome Cocaine embryofetopathy Fetal hydantoin syndrome Kabuki syndrome Fetal trimethadione syndrome Vitamin K antagonist embryofetopathy Fetal alcohol syndrome Lethal occipital encephalocele-skeletal dysplasia syndrome Shprintzen-Goldberg syndrome Fetal methylmercury syndrome Cardiocranial syndrome, Pfeiffer type Fetal minoxidil syndrome Phenobarbital embryopathy Stickler syndrome Toluene embryopathy Methimazole embryofetopathy Cranioectodermal dysplasia Pierre Robin syndrome associated with collagen disease Non-syndromic bilambdoid and sagittal craniosynostosis Diabetic embryopathy Cantú syndrome Pierre Robin syndrome associated with a chromosomal anomaly Teebi-Shaltout syndrome Frontofacionasal dysplasia Rare disease with Pierre Robin syndrome SPECC1L-related hypertelorism syndrome Isolated oxycephaly Carpenter syndrome Craniofrontonasal dysplasia Autosomal recessive Stickler syndrome Craniofrontonasal dysplasia-Poland anomaly syndrome Oculomaxillofacial dysostosis 22q11.2 deletion syndrome TARP syndrome Fetal parvovirus syndrome Craniomicromelic syndrome Pierre Robin syndrome associated with branchial archs anomalies Isolated cloverleaf skull syndrome Oculoauriculofrontonasal syndrome Pierre Robin syndrome associated with bone disease Dysostosis with predominant craniofacial involvement Craniosynostosis, Philadelphia type Maternal phenylketonuria Craniotelencephalic dysplasia Pfeiffer syndrome Frontorhiny Teratogenic Pierre Robin syndrome Craniosynostosis-cataract syndrome Waardenburg syndrome Craniosynostosis Pseudoaminopterin syndrome Craniosynostosis-fibular aplasia syndrome Maternal hyperthermia-induced birth defects X-linked intellectual disability-plagiocephaly syndrome Craniosynostosis-dysmorphism-brachydactyly syndrome Isolated Pierre Robin syndrome Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome Familial scaphocephaly syndrome Syndrome de Jackson-Weiss Craniosynostose type Boston Craniosynostose sagittale non syndromique Ostéodysplasie familiale type Anderson Craniosynostose-anomalies dentaires Scaphocéphalie familiale type McGillivray Syndrome de Treacher-Collins Plagiocéphalie isolée Craniosynostose bicoronale non syndromique Syndrome de crâne en trèfle-dysplasie asphyxiante du thorax Syndrome de Curry-Jones Dysplasie frontonasale acromélique Trouble rare de la succion/déglutition Syndrome de cutis gyrata-acanthosis nigricans-craniosynostose Syndrome de Goodman Syndrome de Cornelia de Lange Syndrome de dysplasie frontonasale-alopécie-anomalies génitales Syndrome de Crouzon Syndrome de Summitt Syndrome de dysplasie frontonasale-microphtalmie sévère-fente faciale sévère Dysplasie cranio-lenticulo-suturale Dysplasie de Kniest Syndrome de Muenke Syndrome C Syndrome d'Antley-Bixler Syndrome de Pai Syndrome d'Apert Maladie néoplasique rare Syndrome de craniosynostose-calcifications intracrâniennes Syndrome de Stickler type 2 Syndrome de dysostose mandibulo-faciale-macroblépharon-macrostomie Syndrome cranio-facio-fronto-digital Syndrome de l'X fragile Syndrome de Stickler type 1 Hyperplasie congénitale des surrénales par déficit en cytochrome P450 oxydoréductase Syndrome de Lowry-MacLean Encéphalocèle nasale Syndrome de trigonocéphalie-anomalies des extrémités Syndrome de craniosynostose-anomalies anales-porokératose Craniosynostose métopique non syndromique Spectre oculo-auriculo-vertébral avec anomalies radiales Syndrome de Hunter-McAlpine Syndrome de trigonocéphalie-petite taille-retard de croissance Acro-céphalo-polydactylie Atélostéogenèse type I Craniosynostose de Herrmann-Opitz Syndrome des synostoses multiples