Poland syndrome.

همراهی نشانگان پولند با اختلال درخودماندگی: گزارش موردی

Objectives: The aim of the current study was to report associated problems of Poland Syndrome in a patient. Method: A 5 years old son affected to Poland Syndrome was accurately assessed. Results: The results showed the patient had communication, verbal and behavioral problems besides Poland Syndrome. Also, he received attention deficit hyperactivity disorder diagnosis and had seizure history. A...

Poland syndrome with dextrocardia and congenital heart disease: A case report

The Poland syndrome is a rare anomaly. It consists of unilateral absence or hypoplasia of the pectoralis muscle, most frequently involving the sternocostal portion and a variable degree of ipsilateral hand and digit anomalies. The combination of Poland syndrome and dextrocardia is uncommon. We describe a case of Poland syndrome with dextrocardia and Patent ductus arteriosus.

Poland’s Syndrome: a Cadaver Case Study

We observed a rare variant case of Poland syndrome in a 55-year-old male cadaver in gross anatomy dissection room at department of Anatomy school of Medicine. His past and family history was not remarkable. The outward appearance of anterior thoracic wall, deltoid and shoulder regions revealed obvious abnormalities. Upon dissection, the following features were observed: (1) On the right side, t...

An unusual case report showing overlapping Features of Poland and Moebius syndrome

[email protected] Phone no. +91 9501544877 Abstract Moebius and Poland syndromes are rare congenital anomalies. Poland syndrome (PS) is characterized by unilateral aplasia/hypoplasia of the breast and pectoralis muscle and ipsilateral deformities in the extremities. However, Moebius-Poland syndrome is rarer than the isolated syndromic conditions. Moebius syndrome is characterized by unilateral...

Mobius Syndrome and Poland Syndrome Presenting Together in a Single Patient

Multiple cavernous malformations presenting in a patient with Poland syndrome: A case report

INTRODUCTION Poland syndrome is a congenital disorder related to chest and hand anomalies on one side of the body. Its etiology remains unclear, with an ipsilateral vascular alteration (of unknown origin) to the subclavian artery in early embryogenesis being the currently accepted theory. Cavernous malformations are vascular hamartomas, which have been linked to a genetic etiology, particularly...