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Documents Cutis aplasia

Sheet 1 of 2 Ref: 2016F0961 © GOSH NHS Foundation Trust April 2016 What is cutis aplasia? Cutis aplasia is a term used to describe an area of skin that has not formed

Documents APLASIA CUTIS CONGENITA OF THE SCALP

APLASIA CUTIS CONGENITA OF THE SCALP Joacil C. da Silva¹, João Paulo C. de Almeida2, Suzana Serra¹, Igor Faquini¹, Saul Quinino¹, Francisco Nêuton

Documents Congenital patellar aplasia in conjunction with trisomy 8. A case report

untitledCASE REPORTActa Orthop. Belg., 2004, 70, 373-376 Congenital patellar aplasia and hypoplasia are quite rare. Bilateral flexion deformity of the fifth finger, patellar

Documents Localization of a Gene for Familial Patella Aplasia-Hypoplasia (PTLAH) to Chromosome 17q21–22

441 Localization of a Gene for Familial Patella Aplasia-Hypoplasia (PTLAH) to Chromosome 17q21–22 Massimo Mangino,1 Otto Sanchez,2 Isabella Torrente,1 Alessandro De

Documents Red cell aplasia in children

Annotations Red cell aplasia in children Red cell aplasia in children is a condition character- ised by failure of erythropoiesis, with normal production of white blood cells

Documents Thumb Hypoplasia and Aplasia

EDUCATION AND TAKE-HOME INSTRUCTION Thumb Hypoplasia and Aplasia What is thumb hypoplasia and aplasia? Thumb hypoplasia, also commonly called hypoplastic thumb, means that

Documents Pure red cell aplasia associated with Systemic Lupus Erythematosus

Normas265 CASO CLÍNICO 1. Núcleo de Medicina Tropical do Pará 2. Universidade do Estado do Pará 3. Universidade Federal do Pará 4. Michigan

Documents Pure Red Cell Aplasia and Thymoma

Pure Red Cell Aplasia and ThymomaCarrie A. Thompson, MD In this issue of the Journal, van der Marel et al.1 report a case of pure red cell aplasia (PRCA) and hypogammaglobulinemia

Documents Aplasia Cutis Congenita of Scalp and Back: A Rare Entity

Aplasia Cutis Congenita of Scalp and Back: A Rare EntityAplasia Cutis Congenita of Scalp and Back: A Rare Entity OPEN ACCESS Urology & Renal Transplantation, S.G Corporate

Documents Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia,...

Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation