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Results 1 - 10 of 63 for dysmorphisms
  1. Congenital cataracts, facial dysmorphism, and neuropathy (CCFDN) is a rare disorder that affects several parts of the body. It is characterized by a ...
  2. Congenital Abnormalities (American Academy of Pediatrics)  
    Birth Defects/Start Here ... Birth Defects ... American Academy of Pediatrics
  3. ... disorder in their family. Birk-Barel mental retardation dysmorphism syndrome Birk-Barel syndrome Intellectual disability, Birk-Barel type Intellectual disability-hypotonia-facial dysmorphism syndrome Mental retardation with hypotonia and facial dysmorphism ...
  4. ClinicalTrials.gov: Congenital Abnormalities From the National Institutes of Health (National Institutes of Health)  
    Birth Defects/Clinical Trials ... Birth Defects ... National Institutes of Health ... From the National Institutes of Health
  5. ... family. Absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardation GPS Genetic Testing Registry: Genitopatellar ...
  6. ... BMKS Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome Oculo-oto-facial dysplasia Oculootofacial dysplasia OOFD ... Registry: Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome Burn-McKeown syndrome National Organization for Rare ...
  7. ... of the condition. Cerebrofaciothoracic dysplasia CFSMR CFTD Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Pascual-Castroviejo ...
  8. ... in their family. Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits Genetic Testing Registry: Char ...
  9. ... Macrocephaly, seizures, intellectual disability, umbilical hernia, and facial dysmorphism Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome ...
  10. 17q12 deletion syndrome is a condition that results from the deletion of a small piece of chromosome 17 in each cell. The deletion occurs on the long (q) arm ...
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