M Tariq, Z Azeem, G Ali, MS Chishti, W … - British Medical Journal, 2009 - jmg.bmj.com Background: Isolated congenital nail clubbing (ICNC) is a rare autosomal
recessive disorder characterised by enlargement of the terminal segments of
fingers and toes with thickened nails due to proliferation of the ... Cited by 2 - Related articles - All 4 versions
M Saghafi, A Azarian, N Nohesara - Rheumatology International, 2008 - Springer Abstract Primary hypertrophic osteoarthropathy or pach- ydermoperiostosis is a
rare congenital disease characterized by clubbing of the fingers, periostitis of
the distal long bones, and hypertrophic skin changes (pachydermia) ... Cited by 3 - Related articles - BL Direct - All 3 versions
KG Coggins, TM Coffman, BH Koller - Nature Genetics, 2008 - nature.com Digital clubbing has been recognized since the time of the ancient Greeks as a
sign of systemic disease. Now, a new study identifies a role for prostaglandin
E2 in the pathogenesis of digital clubbing observed in familial ... Cited by 3 - Related articles - BL Direct - All 3 versions
C Hugosson, S Bahabri, A Rifai, A Al-Dalaan - Pediatric radiology, 1995 - Springer Hypertrophic osteoarthropathy (HOA) characterized by clubbing of fingers and
toes, proliferative periosti- tis of the long bones and oligo- or polysynovitis
is an uncommon condi- tion in children. The primary condition is rare and ... Cited by 3 - Related articles - BL Direct - All 3 versions
T Dabir, AM Sills, CM Hall, C Bennett, LC … - Clinical Dysmorphology, 2007 - journals.lww.com Primary hypertrophic osteoarthropathy is a condition characterized by clubbing,
arthropathy and periostosis of long tubular bones. Three variants of primary
hypertrophic osteoarthropathy are distinguished: pachydermoperiostosis, ... Cited by 3 - Related articles - BL Direct - All 2 versions
S O'Connell, M Suri, D Duff, J Kelleher, CM … - Clinical Dysmorphology, 2004 - journals.lww.com Cranio-osteoarthropathy is a rare condition. Classically, signs are identifiable
in infancy with clubbing of fingers, and delayed closure of the clinically
enlarged cranial sutures, followed by periosteal new bone formation on ... Cited by 3 - Related articles - BL Direct - All 2 versions
A Arivazhagan, P Pandey, B Anandh, RG … - Surgical Neurology, 2009 - Elsevier A 20-year-old man who presented with fever, headache, and vomiting of short
duration was diagnosed as having right parietal abscess and underwent burr hole
and tapping and antibiotic treatment. He later presented with many episodes ... Cited by 3 - Related articles - All 2 versions
P Pillet, F Boralevi, JF Chateil, E Pinlou, D … - Archives de pédiatrie: organe officiel de la Sociéte …, 2002 - ncbi.nlm.nih.gov CASE REPORT: Two brothers with a Currarino's disease are reported. Patients
characteristics included a dysmorphic syndrome, cranial suture defects,
hypertrophic osteoarthropathy and severe chronic eczema. COMMENTS: ... Cited by 3 - Related articles - All 2 versions
SG West, RE Gilbreath, OJ Lawless - Jama, 1981 - Am Med Assoc You are seeing this message because your Web browser does not support basic Web
standards. Find out more about why this message is appearing and what you can do
to make your experience on this site better. ... Add to CiteULike Add to ... Cited by 6 - Related articles - All 2 versions
MM Barraud-Klenovsek, J Lübbe, G Burg - Dermatology(Basel), 1997 - cat.inist.fr The association of hereditary palmoplantar keratoderma and idiopathic clubbing
of the digits in the same patient is uncommon. The differential diagnosis
includes the Bureau-Barrière-Thomas syndrome, primary ... Cited by 4 - Related articles - BL Direct - All 4 versions
