Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Aryeh Metzker"'
Publikováno v:
Acta Dermato-Venereologica. 102:adv00707
Segmental pigmentation disorder (SPD) is characterized by hypo- or hyper-pigmented patches segmentally distributed, present in infancy, more prominently in darker-skinned children. The aim of this study was to define the demographic and clinical char
Autor:
Mordechai Choder, Aryeh Metzker, Dan Geiger, Gabriele Richard, Eli Sprecher, Reuven Bergman, Ilana Chefetz, Orit Topaz, Yoram Altschuler, Margarita Indelman, Dani Bercovich, Jouni Uitto
Publikováno v:
The American Journal of Human Genetics. 79(4):759-764
Familial tumoral calcinosis (FTC) is a rare autosomal recessive disorder characterized by the progressive deposition of calcified masses in cutaneous and subcutaneous tissues, which results in painful ulcerative lesions and severe skin and bone infec
Publikováno v:
Pediatric Dermatology. 15:97-102
Palmoplantar eccrine hidradenitis (PEH) is characterized by painful erythematous papules and nodules of abrupt onset on the soles of young individuals. The histologic hallmark is a predominant neutrophilic infiltrate surrounding the eccrine gland app
Publikováno v:
Pediatric Dermatology. 12:39-42
A 9-month-old infant had pyoderma gangrenosum (PG) and sterile osteomyelitis. Three years later the patient developed Takayasu arteritis (TA). Sterile osteomyelitis was reported in approximately 30 patients with different skin lesions, but never toge
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology. 77:158-166
Intraoral facial and laryngeal features of tumoral calcinosis are reviewed in six patients of Jewish-Yemenite descent. Extraoral features included calcified masses, erythematous patches, and angular cheilitis. Oral soft tissue findings included papil
Publikováno v:
European Journal of Pediatrics. 160:189-191
Idiopathic palmoplantar eccrine hidradenitis (IPPH) is a recently described disorder characterized by painful erythematous plantar nodules and in three cases, showed a typical neutrophilic infiltrate around and within the eccrine sweat apparatus. Fiv
Publikováno v:
American Journal of Medical Genetics. 43:764-767
The syndrome of Albright hereditary osteodystrophy (AHO), pseudohypoparathyroidism (PHP) and pseudopseudohypoparathyroidism (PPHP) is clinically and genetically heterogeneous. Classically, patients with PHP have the skeletal features of AHO, resistan
Autor:
Michael Schwartz, Dan Ben-Amitai, Shmuel Davidson, Dario Prais, Raanan Shamir, Paul Merlob, Aryeh Metzker
Publikováno v:
Pediatric Dermatology. 17:469-471
Neonates with midline lumbar, thoracic, or occipital cutaneous lesions should be suspected of having spinal dysraphism and should undergo an imaging study. The aim of the present study was to evaluate whether sacral nevus flammeus simplex (SNFS) in n
Publikováno v:
The Israel Medical Association journal : IMAJ. 7(5)
Mastocytosis is a heterogeneous group of diseases characterized by the abnormal infiltration of mast cells in the skin and, sometimes, other organs. Some patients may experience symptoms related to mast cell mediator release.To analyze the clinical f
Publikováno v:
Pediatric Dermatology. 13:255-257