## Abstract IMAGe syndrome is a rare condition, first reported by Vilain et al., in 1999, characterized by __i__ntrauterine growth restriction, __m__etaphyseal dysplasia, congenital __a__drenal hypoplasia, and __g__enital anomalies. Patients with this condition may present shortly after birth with
Poland syndrome with bilateral features: Case description with review of the literature
β Scribed by Anwar Baban; Michele Torre; Sebastiano Bianca; Anna Buluggiu; Mario Igor Rossello; Maria Grazia Calevo; Maura Valle; Roberto Ravazzolo; Vincenzo Jasonni; Margherita Lerone
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 194 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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β¦ Synopsis
Abstract
Poland syndrome (PS) has been described as unilateral pectoral muscle deficiency variably associated with ipsilateral thoracic and upper limb anomalies. Bilateral hypoplasia/aplasia of the pectoralis muscle and upper limb defects in association with variable thoracic muscles, chest wall deformities and lower limb defects have been infrequently reported in the literature. We report on a 3Β½βyearβold girl with clinical features consisting in bilateral asymmetric pectoral muscle defects (complete agenesis on the left side and agenesis of the sternocostal head on the right side), nipple hypoplasia, left rib defect, and right hand symbrachydactyly. In this study, we reviewed the bilateral features present in our patient and those described in the literature. Hypotheses explaining bilateral features in PS are reviewed. Β© 2009 WileyβLiss, Inc.
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Myelodysplastic syndrome (MDS) with erythroid hypoplasia/aplasia has not yet been clearly defined, and in most patients it is mistaken for acquired pure red cell aplasia (PRCA). We report a patient with severe transfusion-dependent anemia (Hb 6.9 g/dl) and reticulocytopenia. WBC and platelet counts