Splenogonadal fusion (SGF) is a rare congenital malformation in which the spleen is abnormally connected to the gonad. SGF may occur as an isolated condition or may be associated with other malformations, especially with terminal limb defects in what is called splenogonadal fusion limb defect (SGFLD
Lemierre syndrome: report of five new cases and literature review
β Scribed by David F. Weeks; Douglas S. Katz; Penny Saxon; Wayne S. Kubal
- Publisher
- Springer
- Year
- 2010
- Tongue
- English
- Weight
- 383 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1070-3004
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The neonatal progeroid syndrome (NPS), or Wiedemann-Rautenstrauch, is a rare autosomal recessive disorder comprised of generalized lipoatrophy except for fat pads in the suprabuttock areas, hypotrichosis of the scalp hair, eyebrows, and eyelashes, relative macrocephaly, triangular face, natal teeth,
SPIGELIAN hernia, although not rare, is not a commonly recognized condition and receives scant attention in most of the standard text-books. River (1942) reviewed 116 cases, including 4 of his own, and since that time an increasing number have been reported, but only 29 of these are in the British a
Mental nerve neuropathy, also referred to as numb chin syndrome, is a rare, seemingly harmless symptom. It is more often associated with cancer, either as first symptom or during the outcome, than with benign diseases. In this review, we will focus on www.