Results 1 to 10 of about 81,545 (172)

Poland syndrome accompanied by internal iliac artery supply disruption sequence: a case report

open access: yesJournal of Medical Case Reports, 2018
Background Poland syndrome is a congenital malformation characterized by ipsilateral hand and chest wall depression, including an absence or hypoplasia of the breast and pectoral muscles.
Kenji Gonda   +9 more
doaj   +1 more source

Syndrome de poland: à propos d'un cas et revue de la litterature

open access: yesThe Pan African Medical Journal, 2017
Le syndrome de Poland est une malformation congénitale rare associant à des degrés divers des anomalies thoraciques et du membre supérieur homolatéral. Nous rapportons le cas d'une fillette de 7 ans, explorée pour dépression de l'hémithorax gauche avec ...
Meriam Benzalim   +3 more
doaj   +1 more source

Poland syndrome with associated synbrachydactyly and dextrocardia: a rare case

open access: yes, 2018
Poland’s Syndrome is a rare congenital condition. It is classically characterized by absence of unilateral chest wall muscles and sometimes ipsilateral symbrachydactyly (abnormally short and webbed fingers).
Rajawat, Govind Singh   +2 more
core   +1 more source

A rare case report of Poland syndrome in neonates

open access: yes, 2015
The Poland\u27s anomaly was first described in 1841 by Sir Alfred Poland as a syndrome presenting with absence or underdevelopment of pectoralis major muscle, associated in some cases with a hypoplasia of the breast, an agenesis of 2, 3, 4 and 5 ...
Bhatia, Manvi   +2 more
core   +1 more source

Chronic Fatigue Associated with Post-COVID Syndrome versus Transient Fatigue Caused by High-Intensity Exercise: Are They Comparable in Terms of Vascular Effects?

open access: yesVascular Health and Risk Management, 2022
Michal Chudzik,1,2 Anna Cender,1 Robert Mordaka,1 Jacek Zielinski,3 Joanna Katarzynska,4 Andrzej Marcinek,4,5 Jerzy Gebicki4,5 1Medical Center, Saint Family Hospital, Lodz, Poland; 2Department of Internal Medicine and Geronto-Cardiology, Medical Centre ...
Chudzik M   +6 more
doaj  

Poland Syndrome: A Case Report

open access: yesIndian Journal of Plastic Surgery, 1983
A case of Poland's syndrome characterised by anomalies in the shoulder girdle and symbrachydactyly is reported. First web was also involved. Method of correction adopted by us is described.
Satya Parkash, Santosh Pai
doaj   +1 more source

Poland-Mobius syndrome in an infant girl

open access: yesAnnals of Saudi Medicine, 2009
Mobius syndrome is a rare condition of unclear origin, characterized by a unilateral or bilateral congenital facial weakness with impairment of ocular abduction, which is frequently associated with limb anomalies .
Al-Mazrou Khalid   +2 more
doaj  

Institutional and policy analysis of river basin management: the Warta River Basin, Poland [PDF]

open access: yes
The authors describe and analyze the emergence of river basin management in the Warta River Basin of Poland. The Warta basin's 55,193 km2 cover approximately one-sixth of Poland, and the Warta is a principal tributary to the Oder. Water management issues
Blomquist, William   +2 more
core  

A Rare Case of Poland Syndrome with Absence of Ipsilateral Nasolacrimal Duct [PDF]

open access: yesIndian Journal of Physical Medicine & Rehabilitation, 2008
First described in a cadaver examined by A. Poland atGuy’s Hospital in 1841, “this combined anomaly of webbedfingers(cutaneous syndactyly) of the hand on the sameside and the absence or underdevelopment of the sternocostalportion of ipsilateral ...
Gupta AK   +5 more
doaj  

The Relationship Between the Metabolic Syndrome and the Place of Residence in the Local Community on the Example of the Janów Lubelski District in Eastern Poland: A Population-Based Study

open access: yesDiabetes, Metabolic Syndrome and Obesity, 2021
Grzegorz Józef Nowicki,1 Barbara Ślusarska,1 Katarzyna Naylor,2 Andrzej Prystupa,3 Ewa Rudnicka-Drożak,4 Ulyana Halyuk,5 Petro Pokotylo5 1Department of Family Medicine and Community Nursing, Medical University of Lublin, Lublin, Poland ...
Nowicki GJ   +6 more
doaj  

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