Pierre Robin Syndrome: Causes & Reasons

Possible Causes for Pierre Robin Syndrome

Synonyms: Pierre Robin syndrome (PRS), Pierre Robin anomaly/anomalad, Pierre Robin malformation (PRM) complex, Robin sequence, Robin complex Related conditions - these may [patient.info]

The present patient had typical findings of Nager syndrome and Pierre Robin sequence. [ncbi.nlm.nih.gov]

PIERRE ROBIN ANOMALAD / SYNDROME Robin sequence previously known as Pierre Robin syndrome and Pierre Robin anomalad consists of three essential components: Micrognathia or [fetalultrasound.com]

Non-Syndromic Ocular Stickler Syndrome Type 1

Pierre Robin syndrome and sensorineural deafness associated in 10% of cases. [accessanesthesiology.mhmedical.com]

OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; OSMEDA Is also known as osmed, heterozygous|weissenbacher-zweymuller syndrome|pierre robin syndrome with fetal chondrodysplasia [mendelian.co]

A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome. [en.wikipedia.org]

Congenital Mandibular Hypoplasia

Pierre Robin syndrome. Preoperative appearance. Pierre Robin syndrome. Preoperative appearance. [emedicine.medscape.com]

Juvenile idiopathic arthritis Marfan syndrome Noonan syndrome Pierre Robin syndrome Prader–Willi syndrome Progeria Silver–Russell syndrome Seckel syndrome Smith–Lemli–Opitz [en.wikipedia.org]

Pierre Robin syndrome and mandibulofacial dysostosis versus isolated mandibular hypoplasia Pierre Robin syndrome and MFD syndromes are both defects of the branchial arches [jofs.in]

High Myopia-Sensorineural Deafness Syndrome

Orofacial Structure The most severe problem associated with Stickler syndrome is Pierre Robin syndrome. [wikidoc.org]

Orofacial Structure [ edit ] The most severe problem associated with Stickler syndrome is Pierre Robin syndrome. [en.wikipedia.org]

MIM Entry: 277610 Title: #277610 WEISSENBACHER-ZWEYMULLER SYNDROME; WZS ;;PIERRE ROBIN SYNDROME WITH FETAL CHONDRODYSPLASIA Text: A number sign (#) is used with this entry [genome.jp]

Pierre Robin Syndrome

[…] enwiki Pierre Robin syndrome eswiki Síndrome de Pierre Robin euwiki Robinen sindromea frwiki Syndrome de Pierre Robin itwiki Sindrome di Pierre Robin kkwiki Робен синдромы [wikidata.org]

Pierre Robin Syndrome U.S. [ibis-birthdefects.org]

Pierre Robin Syndrome (PRS)  known as Pierre Robin malformation -Pierre Robin anomaly or Pierre Robin anomalad  A congenital condition of facial abnormalities in humans. [slideshare.net]

Micrognathism

The diagnosis of Pierre-Robin syndrome was made postnatally. The possible differential diagnoses and the main complications of retrognathism are reviewed. [link.springer.com]

Abstract Babies with Pierre Robin syndrome have serious life-threatening risks because of acute respiratory distress and difficult airway management. [ncbi.nlm.nih.gov]

Stickler Syndrome

A child with Pierre Robin syndrome had a family history of Stickler syndrome on the father's side and congenital cataracts on the mother's side. [jamanetwork.com]

An image depicting Pierre Robin syndrome can be seen below. A 5-month-old baby with Pierre Robin sequence and severe micrognathia. [emedicine.medscape.com]

Congenital Aural Atresia

Goldenhaar (hemifacial microsomia), Pfeiffer, Treacher Collins, and Pierre Robin syndromes may be associated with external ear anomalies. [advancedradteaching.com]

[…] canal atresia 2 : Crouzon syndrome Treacher Collins syndrome Goldenhar syndrome Pierre Robin syndrome CT High resolution bony CT reformats is the modality of choice for assessing [radiopaedia.org]

Their proband had Pierre-Robin syndrome [11]. 5. [sonoworld.com]

Pfeiffer-Palm-Teller Syndrome

Robin nanism polydactyly Pierre Robin, sequence of Pierre Robin sequence of faciodigitale anomaly Pierre Robin syndrome chondrodysplasy Pierre Robin, syndrome of Pierre Robin [wikipedia.qwika.com]

syndrome fetal chondrodysplasia Pierre Robin syndrome hyperphalangy clinodactyly Pierre Robin syndrome skeletal dysplasia polydactyly Pignata guarino syndrome Pili torti [en.wikipedia.org]

Pierre Robin syndrome fetal chondrodysplasia[?] Pierre Robin syndrome hyperphalangy clinodactyly[?] Pierre Robin syndrome skeletal dysplasia polydactyly[?] [encyclopedia.kids.net.au]

Cerebro-Costo-Mandibular Syndrome

Cerebro–costo–mandibular syndrome CCM syndrome rib gaps micrognathia Pierre Robin syndrome Persistent link APA Author BIBTEX Harvard Standard RIS Vancouver [research-information.bris.ac.uk]

Carey et al. [1982] coined the term Pierre Robin syndrome or sequence (PRS). [karger.com]

In Pierre-Robin syndrome, the life span is normal. [todaysrdh.com]

Prata-Libéral-Gonçalves Syndrome

Pierre Robin sequence faciodigital anomaly Pierre Robin syndrome fetal chondrodysplasia Pierre Robin syndrome hyperphalangy clinodactyly Pierre Robin syndrome skeletal dysplasia [mindmappedia.com]

[…] ataxia Pierre Robin sequence congenital heart defect talipes Pierre Robin sequence faciodigital anomaly Pierre Robin syndrome fetal chondrodysplasia Pierre Robin syndrome [bioreference.net]

Coxoauricular Syndrome

An image depicting Pierre Robin syndrome can be seen below. A 5-month-old baby with Pierre Robin sequence and severe micrognathia. [emedicine.medscape.com]

Robin syndrome 6 Cases 1484 Contractures-ectodermal dysplasia-cleft lip/palate syndrome 2 Cases 314002 Contractures-webbed neck- micrognathia-hypoplastic nipples syndrome [azkurs.org]

[…] conductive hearing loss hypermobile middle ear systems Skeletal joint hypermobility mild spondyloepiphyseal dysplasia precocious osteoarthritis Siehe auch: Mikrognathie Pierre-Robin-Sequenz [pacs.de]

Acrocephalopolysyndactyly

pierre robin Pierre robin Syndrome pierre robin Syndrome polymalformatif apert Syndrome pfeiffer Maladie apert Syndrome polymalformatif schinzel-giedion Syndrome schinzel-giedion [medcode.ch]

paralytic (complete) (incomplete) - G83.9 - oculofacial, congenital (Moebius) - Q87.0 - Pierre Robin deformity or syndrome - Q87.0 - Robin (-Pierre) syndrome - Q87.0 - Syndrome [icdlist.com]

congenital Q87.0 (Moebius) Pierre Robin deformity or syndrome Q87.0 Robin Q87.0 (-Pierre) Syndrome - see also Disease congenital facial diplegia Q87.0 oculo-auriculovertebral [icd10data.com]

Patterson Pseudoleprechaunism Syndrome

Robin syndrome hyperphalangy clinodactyly Pierre Robin syndrome skeletal dysplasia polydactyly Pierre Robin's sequence Pigmentary retinopathy Pigment-dispersion syndrome [bionity.com]

Stickler Syndrome Type 5

An image depicting Pierre Robin syndrome can be seen below. A 5-month-old baby with Pierre Robin sequence and severe micrognathia. [emedicine.medscape.com]

A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome. [en.wikipedia.org]

In 1926, Pierre Robin published the case of an infant with the complete syndrome. [emedicine.medscape.com]

Autosomal Dominant Oto-Spondylo-Megaepiphyseal Dysplasia

MIM Entry: 277610 Title: #277610 WEISSENBACHER-ZWEYMULLER SYNDROME; WZS ;;PIERRE ROBIN SYNDROME WITH FETAL CHONDRODYSPLASIA Text: A number sign (#) is used with this entry [genome.jp]

A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome. [en.wikipedia.org]

A particular group of physical features called Pierre Robin sequence is also common in people with Stickler syndrome. [ghr.nlm.nih.gov]

Familial Median Cleft of the Upper and Lower Lips

192430 AD Pierre Robin syndrome, cleft palate, small open mouth, myopathic facies, retrognathia, prominent nose with squared-off nasal tip UNK Treacle TCOF1 5q32-q33.1 154500 [en.wikibooks.org]

Part of chromosomal abnormalities : Pierre Robin sequence, Patau syndrome ( trisomy 13 ), Edwards syndrome ( trisomy 18 ) Environmental factors : exposure to teratogenic substances [amboss.com]

• 3q29 microdeletion syndrome. • Pierre Robin sequence. • Trisomy 18 (Edwards' syndrome), trisomy 13 (Patau's syndrome) and trisomy 15. • Van der Woude syndrome. 5. [article.sciencepublishinggroup.com]

Stickler Syndrome Type 2

A particular group of physical features, called the Pierre Robin sequence, is common in children with Stickler syndrome. [en.wikipedia.org]

The Stickler syndrome. N Engl J Med1972;286:546–7. Schreiner RL, McAlister WH, Marshall RE, Shearer WT. Stickler syndrome in a pedigree of Pierre Robin syndrome. [jmg.bmj.com]

a possible presentation of Pierre Robin sequence. ( 30709837 ) Briosa F...Oom P 2019 3 Floppy eyelid syndrome in stickler syndrome. ( 30775613 ) Sun SY...Chen JJ 2019 4 [malacards.org]

Acrorenal Mandibular Syndrome

syndrome 150230 Glossoptosis, micrognathia and cleft palate syndrome Pierre-Robin syndrome 261800 Goltz-Gorlin syndrome Basal cell nevus 109400 Hallerman-Streiff syndrome [keratin.com]

Previously known as 'Pierre Robin syndrome', the way this diagnostic entity is viewed is now undergoing change. [readbyqxmd.com]

Cleft of Hard Palate

Robin syndrome. [columbiasurgery.org]

Conclusion: retrognatism, suspicion of Pierre-Robin syndrome, suspicion of small posterior palate defect Figure 6. Figure 6. Abnormal profile. [medichub.ro]

Pierre Robin Syndrome Stickler Syndrome Treacher Collins Syndrome Van Der Woude Syndrome What Does It Affect? [home-speech-home.com]

Gorlin-Psaume Syndrome

Yes 1 Exempt from POA reporting No The ICD code Q870 is used to code Pierre Robin syndrome Pierre Robin syndrome (abbreviated to PRS, and also known as Pierre Robin malformation [icd.codes]

Ectopia Lentis

[…] dysostosis Wildervanck syndrome Conradi syndrome Pfaundler syndrome Crouzon syndrome Pierre Robin syndrome Sprengel deformity Video Ectopia Lentis Surgery This 46 year old [retinavitreous.com]

Crouzon’s disease; Refsum syndrome; Kniest syndrome; Mandibulofacial dysostosis; Sturge-Weber syndrome; Conradi syndrome; Pfaundler syndrome; Pierre Robin syndrome; Wildervanck [emergency-live.com]

Crouzon syndrome Pierre Robin syndrome Sprengel deformity History A history of any recent trauma is of principal importance. [eyewiki.aao.org]

Diamond-Blackfan Anemia Type 2

Over half of all DBA patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and [orpha.net]

Pierre-Robin syndrome, congenital glaucoma, and cataracts have also been described. [symptoma.com]

Treacher-Collins Syndrome

Pierre Robin syndrome. Preoperative appearance. Pierre Robin syndrome. Preoperative appearance. [emedicine.com]

[…] an increased risk of malignancy. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin [uniprot.org]

More recently, as described for Pierre Robin syndrome, early bilateral mandibular distraction can be performed to correct the airway problem. [emedicine.com]

Acrootoocular Syndrome

Head and face reconstruction (Medical Encyclopedia) Pierre Robin syndrome (Medical Encyclopedia) [ Read More ] [icdlist.com]

Pierre-Robin syndrome associated with Chiari type I malformation. [link.springer.com]

Metaphyseal Acroscyphodysplasia

Sanderson Fraser syndrome 0 *Abnormalities, Multiple *Exophthalmos *Hand Deformities, Congenital *Pierre Robin Syndrome. [reference.md]

Intellectual disability-balding-patella luxation-acromicria syndrome Intellectual disability-brachydactyly-Pierre Robin syndrome Intellectual disability-cataracts-calcified [se-atlas.de]

1: 279 Pierre-Robin sequence, 2: 922–925 Micromelia achondrogenesis, 1: 15 thanatophoric dysplasia, 2: 1130 Microphthalmia with linear skin defects, 2:741–743 Aicardi syndrome [studfiles.net]

Pseudoaminopterin Syndrome

Robin syndrome hyperphalangy clinodactyly Pierre Robin syndrome skeletal dysplasia polydactyly Pierre Robin's sequence Pigmentary retinopathy Pigment-dispersion syndrome [wikidoc.org]

宇佐美真一 498 255 pharynx/larynx hypoplasia-omphalocele, Shprintzen-Goldberg type 石田　修一 500 256 phenylketonuria 岡野　善行 502 257 Pierre Robin syndrome(Robin sequence) 中山　英樹上巻 258 [nippon-rinsho.co.jp]

X-Linked Mandibulofacial Dysostosis

192430 AD Pierre Robin syndrome, cleft palate, small open mouth, myopathic facies, retrognathia, prominent nose with squared-off nasal tip UNK Treacle TCOF1 5q32-q33.1 154500 [widesmiles2.org]

[…] in 50-80% of cases, most commonly Stickler & VCF syndromes 19 Pierre-Robin Sequence Figure Robin sequence. [slideplayer.com]

188400 AD low-set ears, short ears, small mouth, submucous or overt palatal cleft, cleft lip, bulbous nose, square nasal tip, short philtrum, micrognathia, Velocardiofacial syndrome [widesmiles2.org]

Adactyly of Foot

[…] claw deformity, macrodactyly, malaligned toes, obstetrical ultrasound, oligodactyly, Pierre Robin syndrome, polydactyly, polysyndactyly, Robinow syndrome, rocker bottom foot [sonoworld.com]

50 photophobia, 255 Pierre Robin syndrome, 362 plagiocephaly, 99 Poland sequence, 99 Poland syndrome, 173, 297, 397, 443 pollex abductus anomaly, 307, 422 pollicization, [docplayer.net]

Charge syndrome, cleched hand, clinidactyly, club hand, clubfoot, ectrodactyly, FADS, fetal akinesia deformation sequence, fetal feet, fetal hands, fetal ultrasound, lobster [sonoworld.com]

Kniest Dysplasia

Cleft palate (sometimes associated with Pierre-Robin syndrome, see this term), kyphoscoliosis, premature osteoarthritis, severe myopia and deafness are common findings. [orpha.net]

Cleft palate (sometimes associated with Pierre-Robin syndrome), kyphoscoliosis, premature osteoarthritis, severe myopia, and deafness are common features. [issuu.com]