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Differential Diagnosis For Long thin fingers/toes (arachnodactyly)

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Long thin fingers/toes (arachnodactyly)
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Neoplastic Disorders: Endocrine adenoma syndrome 2B/MEA IIB
Metabolic, Storage Disorders: Homocystinuria/homocystinemia
Congenital, Developmental Disorders: Shprintzen-Goldberg craniosynostosis syndrome (15q21.1); Beals/arachnodactyly syndrome; Velocardiofacial (22q gene) syndrome
Hereditary, Familial, Genetic Disorders: Marfan's syndrome; Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3); Papillion-Lefevre syndrome; Craniofrontonasal Syndrome (CFNS); Loeys-Dietz Syndrome; Neuhauser Syndrome
Reference to Organ System: Osteopathia striata with cranial stenosis
Drugs: Fetal Valproate/Valproic Syndrome
Synonyms: Arachnodactylies, Arachnodactyly, Arachnodactyly ((congenital)), Arachnodactyly (disorder), Congenital arachnodactyly, Dolichostenomelia, fingers spider, HAND SPIDERLIKE, Spider finger, spider fingers
Definition: Be the first to add a definition for Long thin fingers/toes (arachnodactyly)
External Links Related to Long thin fingers/toes (arachnodactyly): Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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