Medicine:Benjamin syndrome
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| Benjamin syndrome | |
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| Other names | Benjamin anemia |
Benjamin syndrome is a type of multiple congenital anomaly/intellectual disability (MCA/MR) syndrome. It is characterized by hypochromic anemia with intellectual disability and various craniofacial and other anomalies.[1] It can also include heart murmur, dental caries and splenic tumors.[2]
It was first described in the medical literature in 1911.[3] Symptoms include megalocephaly, external ear deformities, dental caries, micromelia, hypoplastic bone deformities, hypogonadism, hypochromic anemia with occasional tumors, and intellectual disability.[4]
References
- ↑ Firkin, Barry G.; Whitworth, Judith A. (2001). Dictionary of medical eponyms (2nd ed.). Informa Health Care. p. 30. ISBN 978-1-85070-333-4. https://archive.org/details/dictionaryofmedi0000firk/page/30.
- ↑ Bartolucci, Susan L; Stedman, Thomas Lathrop; Forbis, Pat (2005). Stedman's medical eponyms (2nd ed.). Lippincott Williams & Wilkins. p. 63. ISBN 978-0-7817-5443-9.
- ↑ Benjamin E (1911). Über eine selbständige Form der Anämie im frühen Kindersalter. Verh Deut Ges Kinderh, 1911,119-24.
- ↑ Jablonski, Stanley (1991). Jablonski's dictionary of syndromes & eponymic diseases. Krieger Pub. Co. ISBN:978-0-89464-224-1
External links
- Benjamin syndrome via National Library of Medicine.
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