introduction camurati-engelmann disease (ced) is a rare autosomal dominant disease with various phenotypic expressions. the symptoms usually develop during childhood. the hallmark of the disease is bilateral symmetric diaphyseal hyperostosis of the long bones with progressive involvement of the metaphysis. the epiphysis is strictly spared. the common clinical symptoms are pain of the extremitie...

1Resident Physician at Hospital Estadual Vila Alpina/Diagnostic Imaging Service II, associated with the Luiz Roberto Barata Barradas Specialist Medical Outpatient Clinic (AME), São Paulo, SP, Brazil 2Resident Physician at Hospital A.C.Camargo Cancer Center, São Paulo, SP, Brazil 3Orthopedist, Prefeitura Municipal de Barueri, Barueri, SP, Brazil 4Supervising Physician at the Continuing Education...

Frankiastrain CeD is a member ofFrankialineage Ib that is able to reinfect plants of theCasuarinafamilies. Here, we report a 5.0-Mbp draft genome sequence with a G+C content of 70.1% and 3,847 candidate protein-encoding genes.

This 42 year old woman had a history of delayed motor development, chronic muscle fatigue and gait disturbance. Her mother and mother’s brother suffered from similar symptoms. At the age of 20 she was diagnosed with Camurati-Engelmann syndrome. At that time she started to suffer from fluctuating tinnitus in the right ear and attacks of rotational vertigo lasting hours. The vertigo was accompani...

marten using a broom rust in Engelmann spruce as a resting site Figure 29-Brooms caused by spruce broom rust are most conspicuous durmg the summer when yellow-brown spores are present. Figure 28Spruce broom rust on Engelmann spruce.

Camurati-Engelmann disease is a rare autosomal dominant bone dysplasia belonging to the group of craniotubular hyperostoses. Genetic analysis classically shows mutation on TGF?1 gene. A young woman was hospitalized with intense pain in lower limbs, associated radiographic hyperostosis and sclerosis long bones. Mutation LRP6 has recently been high mass. In this case report, missense variant gene...

UNLABELLED Schnitzler's syndrome is a rare disease characterized by a monoclonal IgM (or IgG) paraprotein, a nonpruritic urticarial skin rash, and 2 (or 3) of the following: recurrent fever, objective signs of abnormal bone remodeling, elevated CRP level or leukocytosis, and a neutrophilic infiltrate on skin biopsy. It responds well to treatment with the interleukine-1-inhibitor anakinra. We re...

s: M.G. Spina, K. Langnaese, G.F. Orlando, S.A. Andrabi, T.F.W. Horn, J. Rivier, W. Vale, M.Engelmann and G. Wolf. Urocortin is coexpressed with neuronal nitric oxide synthase in thesupraoptic nucleus but not in the Edinger westphal nucleus of rats.1st Joint French-German NO Meeting, Strassbourg, France (1-4 October, 2003) M.G. Spina, K. Langnaese, G.F. Orlando, S.A. Andrabi, T.F.W....