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         Popliteal Pterygium Syndrome:     more detail
  1. Anomalies And Curiosities Of Medicine- George M. Gould, A.M., M.D. by A.M., M.D. George M. Gould, 2010-02-17

81. Multiple Pterygium Syndrome
Record. syndrome. multiple pterygium syndrome pterygium universale. Summary. A rare syndrome of short stature, abnormal facies and webbing of the neck, antecubital, digital, popliteal
http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome471.html
Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes
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Syndrome multiple pterygium syndrome Synonyms Escobar syndrome familial pterygium syndrome pterygium colli syndrome pterygium syndrome pterygium universale Summary A rare syndrome of short stature, abnormal facies and webbing of the neck, antecubital, digital, popliteal, and intercural areas. Joint contractures, vertebral fusion defects, and rocker-bottom feet are usually associated. Major Features Head and neck: Epicanthal folds and small mandible with pointed receding chin, long philtrum, and syngnathia. Ears: Low-set ears. Eyes: Downslanting palpebral fissures, blepharoptosis, and puffiness about the eyes in some cases. Mouth and oral structures: Downturned angles of the mouth, lip pits, occasional cleft palate, and spoonlike shape of the tongue (lingua cochlearis). Neck: Pterygia. Hand and foot: Soft tissue syndactyly of the fingers, flexion deformity of the fingers and thumbs, talipes calcaneovalgus, and rocker-bottom feet, Extremities: Popliteal pterygia

82. Syndrome, Popliteal Pterygium - Medical Dictionary Definitions Of Popular Medica
MedicineNet Home MedTerms medical dictionary AZ List syndrome, popliteal pterygium. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=5659

83. Birth Disorder Information Directory - P
Pontocerebellar Hypoplasia Type II Support Group. popliteal pterygiumsyndrome See pterygium, syndrome, popliteal. Porencephaly List
http://www.bdid.com/defectp.htm

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P-4 Deletion Syndrome p47-PHOX, Deficiency of p67-PHOX, Deficiency of Pachydermopreiostosis (Hypertrophic Osteoarthropathy, Primary or Idiopathic) Pachyonychia Congenita Pagod Syndrome Pagon Bird Detter Syndrome (Anemia Sideroblastic Spinocerebellar Ataxia) Pagon Syndrome Pallister Syndrome Pallister Hall Syndrome (Hypothalamic Hamartoblastoma, Hypopituitarism, Imperperforate Anus, and Postaxial Polydactyly) Pallister Killian Syndrome

84. TheFetus.net - Pterygium Syndrome Multiple Lethal -Luis A. Izquierdo, MD*, Teres
Associated anomalies. Multiple pterygium syndrome presents with a distinct groupof anomalies (see Table 1). Table 1 Associated Anomalies. q crural. q popliteal.
http://www.thefetus.net/page.php?id=438

85. Conditions And Diseases: Genetic Disorders: Popliteal Pterygium Syndrome| Treasu
Information on Conditions and Diseases, Genetic Disorders, PoplitealPterygium syndrome and much more Treasure Coast Health. Treasure
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86. ORPHANET® Multiple Pterygium Syndrome, Lethal Type
The LMPS is to be distinguished from the lethal popliteal pterygium (Bartsocas Papas)syndrome, where pterygium are limited to the popliteal region and lethal
http://www.orpha.net/static/GB/multiplepterygiumsyndrome.html

87. Article : Case Report - Antenatal Ultrasound Diagnosis Of Multiple Pterygium Syn
in lethal multiple pterygium syndrome is not contractures but fetal edema which isa constant observation in LMPS 2. Limited pterygia of the popliteal region
http://www.ijri.org/articles/archives/2002-12-4/obstetric_555.htm
Obstetric
Case report: Antenatal ultrasound diagnosis of multiple pterygium syndrome
N Bhargava, Lalendra Upreti, S. K. Bhargava, Shashank Jain Ind J Radiol Imag 2002 12:4:555-558 Keywords: Pterygium Syndrome
Introduction Multiple pterygium Syndrome (MPS) is a rare autosomal recessive disorder characterized by multiple flexion contractures with skin webs across the joints, hydrops fetalis, polyhydramnios and hypoplastic lungs. [1] Two types have been described: the classical form appearing in children and adolescents, and the lethal form involving abortuses and stillbirths [1]. Antenatal ultrasound examination can establish the correct diagnosis by identifying the major features. We report a second trimester pregnancy termination in a woman following intra uterine findings of hydrops fetalis, polyhydramnios, lack of fetal movements and short, fixed malformed limbs. Early prenatal diagnosis of this condition is possible using ultrasound as early as in the early second trimester. Multiple etiologies have been described which would be discussed. [2] Figure 1: Longitudinal section of the fetal neck-subcutaneous edema and short neck.

88. CHDD - Behavioral Science Core
220. Dr.Cunningham. Pfeiffer syndrome. 1. Dr.Cunningham. popliteal-pterygium syndrome.1. Dr.Cunningham. Proteus syndrome. 2-20. Dr.Cunningham. Saethre-Chotzen syndrome.
http://depts.washington.edu/chdd/MRDDRC/cores/genetics_cellLine.html

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89. HEDINGER SYNDROME PTERYGIUM POPLITEAL
DEFECT; ULTRASONOGRAPHY; ULTRASONOGRAPHY ABDOMEN; ULTRASONOGRAPHY ABDOMEN KIDNEY;INPATIENT; KIDNEY FAILURE DEFECT; KIDNEY FAILURE; HEDINGER syndrome CELLAR INF
http://www.med.univ-rennes1.fr/cerf/ico_an/IDRE/HADM1540.HTM
CASE indexation ABDOMEN VOLUME INCREASE; DEFICIENCIES; CELLARS; DYSPNEA; DYSPNEA DEFECT; ULTRASONOGRAPHY; ULTRASONOGRAPHY ABDOMEN; ULTRASONOGRAPHY ABDOMEN KIDNEY; INPATIENT; KIDNEY FAILURE DEFECT; KIDNEY FAILURE; HEDINGER SYNDROME CELLAR INF; HEDINGER SYNDROME CELLAR SUP; EXTUMESCENCE; EXTUMESCENCE DEFECT; EXTUMESCENCE VERY BULKY; EXTUMESCENCE BULKY AMYOTROPHY; DEFICIENCIES; DIETHYLSTILBESTROL HEDINGER SYNDROME FEMALE; INPATIENT; DISEASE PYRAMIDAL; MORPHOLOGY FEMININE; MUSCLES ATROPHY DEFECT; MUSCLES ATROPHY LOWER LIMBS; MUSCLES ATROPHY UPPER LIMB; MUSCLES ATROPHY EXTREMITIES; MUSCLES HYPOTROPHY; HEDINGER SYNDROME PYRAMIDAL; HEDINGER SYNDROME PYRAMIDAL DEFECT; HEDINGER SYNDROME PYRAMIDAL G DEFICIENCIES; STATE'DEFECT; STATE GENERAL DAMAGE PROGRESSIVE; STATE GENERAL ALTER; INFLAMMATION DEFECT; HEDINGER SYNDROME INFLAMMATORY; HEDINGER SYNDROME INFLAMMATORY DEFECT; EXTUMESCENCE; EXTUMESCENCE DEFECT; EXTUMESCENCE INFLAMMATORY DEFICIENCIES; EX. NEUROLOGICAL NORMAL; INPATIENT; INPATIENT PEDIATRICS; ICHTHYOSIS-ANOMALY EXTREMITIES; nulliparite; TESTS SHOCK toxi-INFECTIOUS; HAEMATEMESIS; ICHTHYOSIS-ANOMALY EXTREMITIES; POISONING

90. 99-1-5
is named as pterygium syndrome, multiple pterygium syndrome or pterygium colli syndromeis characterized with webbing in the neck, popliteal and antecubital
http://www.cu.edu.tr/fakulteler/tf/tfd/99-1-5.htm
ÇUKUROVA ÜNÝVERSÝTESÝ TIP FAKÜLTESÝ DERGÝSÝ Sayfa: 24-26, Cilt: 24 , Sayý: Multipl pterigium sendromu: bir olgu sunumu Dr.Münevver TÜRKMEN , Dr.Dilara SÜLEYMANOVA Adnan Menderes Üniversitesi Týp Fakültesi Çocuk Saðlýðý ve Hastalýklarý ABD. AYDIN, Ç.Ü. Týp Fakültesi Týbbý Biyoloji ve Genetik ABD. Balcalý/ADANA ÖZET: Pterigium sendromu, multipl pterigium sendromu, pterygium colli sendromu olarak adlandýrýlan bu antite; boyunda, antekubital ve popliteal fossada yelelenme (webbing), göðüs deformiteleri, skolyoz (vertebra anomalileri), sindaktili, kamptodaktili, boy kýsalýðý, min r yüz anomalileri ve yarýk damak ile karakterizedir. Genetik geçiþi konusunda çeþitli görüþler varsa da otosomal resesif kalýtým þekli kabul görmüþtür. Burada akraba evliliði sonucu doðan, dismorfik yüz görünümü, boyunda yelelenme, dirsekler de, omuz, diz ekleminin arkasýnda, kalça ekleminin ön yüzünde deri kývrýmlarý (pterigium) ve göðüs kafesinde deformiteleri, kriptorþidizmi olan multipl pterigium sendromu tanýsý konan bir olgu genetik danýþma verilmesi nedeniyle sunulmuþtur. Anahtar kelimeler: Multipl pterigium sendromu, Otosomal resesif kalýtým

91. The Medword List - Medical Transcription Directory - The Medword List - Conditio
PallisterHall syndrome ( 1 ). Personal Pages ( 2 ). popliteal Pterygiumsyndrome ( 1 ). Prader-Willi syndrome ( 3 ). Propionic Acidemia ( 1 ).
http://www.medwordlist.com/Conditions_and_Diseases/Genetic_Disorders/
Top Level Conditions and Diseases : Genetic Disorders Categories: Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome Alagille Syndrome ... Zellweger Syndrome Links:
  • Genetic and Rare Conditions Site popular
    Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.
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    Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
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    Information on a rare congenital disease.
    http://www.p-c-d.org/en/
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92. A CASE OF A NEW SYNDROME OR A VARIANT OF THE RARE POPLITEAL

http://www.worldscinet.com/jmr/05/0501/S0218957701000428.html
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Journal of Musculoskeletal Research, Vol. 5, No. 1 (2001) 73-77
doi:10.1142/S0218957701000428
A CASE OF A NEW SYNDROME OR A VARIANT OF THE RARE POPLITEAL PTERYGIUM SYNDROME
, Zekeriya Tosun , Mehmet Arazi and M. I. Safa Kapicioglu Department of Orthopedics and Traumatology
e-mail tunccevat@hotmail.com
ABSTRACT The popliteal pterygium syndrome is very rare, and is characterized by a congenital popliteal web accompanying the genitourinary, craniofacial, and musculoskeletal anomalies. We described a case of presumably popliteal pterygium syndrome with severe right popliteal web, right renal agenesis, left bifurcated ninth rib, urethral orifice in the vagina, right presacral discoloration resembling A-V malformation, imperforate anus, skin dimple in the left gluteal region, right calcaneovalgus foot with supernumerary digits and aberrant profunda femoris artery. This is the first report of this combination in the pertinent literature.
Keywords : Knee contracture, Popliteal pterygium, Congenital anomaly

93. Syngnathia And Van Der Woude Syndrome A Case Report And
Fewer than 50 cases have been described, most commonly in association with poplitealpterygium syndrome (facial deformities, cleft lip/palate, lip pits
http://cpcj.allenpress.com/cpcjonline/?request=get-document&doi=10.1597/1545-156

94. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/P
Polydystrophic Oligophrenia@ (6); Pompe Disease@ (4); popliteal PterygiumSyndrome@ (2); Porencephaly@ (4). Porphyrias@ (17); PortalSystemic
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/P
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95. ORPHANET - Rare Diseases - Orphan Drugs
Printing version, DISEASE Bartsocas papas syndrome, Synonym(s) Poplitealpterygium syndrome lethal type, ICD Q87.2, The amnion rupture
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1234

96. Mioti: Diseases + Conditions
Polymyositis. • Polyps, • Pompe Disease. • popliteal PterygiumSyndrome, • Porcupine Man. • Porencephaly, • Pornography Addiction.
http://www.mioti.com/cat/condition/results.asp?Alpha=P

97. SearchBug Directory: Health: Conditions_and_Diseases: Genetic_Disorders: Poplite
Search the Web Web. Open Directory. Search popliteal PterygiumSyndrome,
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Web Pages - ranked by popularity NORD: Popliteal Pterygium Syndrome http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Popliteal%20Pterygium%20Syndrome%20 Offers synonyms, a general discussion and further resources. National Library of Medicine: Multiple Pterygium Syndrome http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome471.html Includes the synonyms, a summary and the major features.
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98. Health Conditions And Diseases Genetic Disorders Popliteal Pterygium Syndrome
Top Health Conditions and Diseases Genetic Disorders popliteal PterygiumSyndrome (2). Top Web Sites National Library of Medicine
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