Pierre Robin Syndrome

Informaţii despre

Nume		Pierre Robin Syndrome
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli fetale; Boli rare
Clasificari ICD10		Congenital malformation syndromes predominantly affecting facial appearance
Clasificare anatomică Malacards		Boli ale ochiului

Vezi şi

Boli A-Z		Adie Pupil Aicardi Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amniotic Band Syndrome Androgen Insensitivity Syndrome, Mild Aneurysm Aniridia 1 Ankyloglossia Anorexia Nervosa 1 Antisynthetase Syndrome Apert Syndrome Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Astrocytoma Blood Group--Ahonen Blood Group, Dombrock System Campomelic Dysplasia Catel-Manzke Syndrome Cerebellar Hypoplasia Cerebrocostomandibular Syndrome Choanal Atresia, Posterior Chromosomal Triplication Chromosome 16p13.3 Duplication Syndrome Cleft Lip Cleft Palate, Isolated Cleft Tongue Congenital Hepatic Fibrosis Congenital Hypoplastic Anemia Congenital Hypothyroidism Congenital Microgastria Congenital Radioulnar Synostosis Crouzon Syndrome Diamond-Blackfan Anemia Diamond-Blackfan Anemia 1 Diamond-Blackfan Anemia 15 with Mandibulofacial Dysostosis Distal Arthrogryposis Dysostosis Ectodermal Dysplasia Esophageal Atresia Fanconi Anemia, Complementation Group E Gastroesophageal Reflux Heart Tumor Hepatic Adenomas, Familial Hepatitis Hyperphalangy Immunoglobulin Switch Sequences Irregular Astigmatism Isolated Pierre Robin Sequence Klippel-Feil Syndrome Laryngitis Lateral Meningocele Syndrome Left Ventricular Noncompaction Lymphoid Interstitial Pneumonia Macrocytic Anemia Mn1 Multiple Sclerosis Nasopharyngeal Teratoma Nasopharyngitis Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Odontoma Oligohydramnios Otitis Media Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant Papillary Tumor of the Pineal Region Periodontitis Pharyngitis Polymorphic Reticulosis Prieto X-Linked Mental Retardation Syndrome Radioulnar Synostosis Sacral Defect with Anterior Meningocele Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sleep Apnea Stickler Syndrome Swallowing Disorders Synostosis Teratoma Tooth Agenesis