Results 1 -
6
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6
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Hypertelorism
- Birth Defects/Specifics ... Birth Defects ... Bone Diseases/Children ... Bone Diseases ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health
- Bile Duct Diseases/Genetics ... Bile Duct Diseases ... Congenital Heart Defects/Genetics ... Congenital Heart Defects ... Genetic and Rare Diseases Information Center ... From ...
- Developmental Disabilities/Specifics ... Developmental Disabilities ... Cri du chat syndrome is a rare genetic condition that is caused by the deletion of genetic ...
- Loeys-Dietz Syndrome (Marfan Foundation)Connective Tissue Disorders/Specifics ... Connective Tissue Disorders ... Marfan Syndrome/Related Issues ... Marfan Syndrome ... Marfan Foundation ... Loeys-Dietz syndrome is ...
- Noonan Syndrome (For Parents) (Nemours Foundation)... Deeply grooved philtrum, undersized lower jaw, LEOPARD syndrome, Hypertelorism, Cardiofaciocutaneous syndrome, Short stature, growth hormone, autosomal dominant, ...
- Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDFCraniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
(Genetic and Rare Diseases Information Center) 