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SyndromeDown SyndromeMetabolic Syndrome XNephrotic SyndromeSjogren's SyndromeTurner SyndromeAbnormalities, MultipleMyelodysplastic SyndromesCushing SyndromeAcute Coronary SyndromePolycystic Ovary SyndromeWilliams SyndromeDiGeorge SyndromeHorner SyndromePrader-Willi SyndromeLong QT SyndromeGuillain-Barre SyndromeHemolytic-Uremic SyndromeCompartment SyndromesTourette SyndromeAntiphospholipid SyndromePorcine Reproductive and Respiratory SyndromeKlinefelter SyndromeCarpal Tunnel SyndromeWerner SyndromeReye SyndromeBartter SyndromePorcine respiratory and reproductive syndrome virusHELLP SyndromeBloom SyndromeBrugada SyndromeEhlers-Danlos SyndromeRespiratory Distress Syndrome, AdultAngelman SyndromePedigreeSevere Acute Respiratory SyndromeRestless Legs SyndromeJob SyndromeWiskott-Aldrich SyndromeMutationParaneoplastic SyndromesSweet SyndromeAcquired Immunodeficiency SyndromeIntellectual DisabilityChurg-Strauss SyndromeSturge-Weber SyndromeBudd-Chiari SyndromePhenotypeChediak-Higashi SyndromeWolff-Parkinson-White SyndromeFaciesKallmann SyndromeSick Sinus SyndromeStevens-Johnson SyndromeSezary SyndromeFelty SyndromeRisk FactorsUsher SyndromesBeckwith-Wiedemann SyndromeAlagille SyndromeTreatment OutcomeBardet-Biedl SyndromeACTH Syndrome, EctopicPeutz-Jeghers SyndromeHemorrhagic Fever with Renal SyndromeOculocerebrorenal SyndromeCockayne SyndromeSmith-Lemli-Opitz SyndromeCraniofacial AbnormalitiesWiskott-Aldrich Syndrome ProteinStiff-Person SyndromeShort Bowel SyndromeBehcet SyndromeInfant, NewbornZollinger-Ellison SyndromeSerotonin SyndromeHepatopulmonary SyndromeOrofaciodigital SyndromesProteus SyndromeDuane Retraction SyndromeImmunologic Deficiency SyndromesComplex Regional Pain SyndromesGoldenhar SyndromeRespiratory Distress Syndrome, NewbornNeuroleptic Malignant SyndromeCostello SyndromeKlippel-Feil SyndromeSubclavian Steal SyndromeHantavirus Pulmonary SyndromeDNA Mutational AnalysisNeoplastic Syndromes, HereditaryFatal OutcomeThoracic Outlet SyndromeHermanski-Pudlak SyndromePregnancyRetrospective StudiesWhite spot syndrome virus 1LEOPARD SyndromeCase-Control StudiesHand Deformities, Congenital

Craniodiaphyseal dysplasia: an unusual cause of recurrent dacryocystitis. (9/24)

We describe a rare syndrome characterized by severe craniofacial hyperostosis, sclerosis, obliteration of paranasal sinuses and foramina of skull base, in a 10-year-old female child who presented with abnormal facial features and recurrent dacryocystitis due to narrowing of nasolacrimal duct.  (+info)

TGF-beta1-induced migration of bone mesenchymal stem cells couples bone resorption with formation. (10/24)

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The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis. (11/24)

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Unusual association between enchondroma and Camurati-Engelmann disease: a case report. (12/24)

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Two distinct regions of latency-associated peptide coordinate stability of the latent transforming growth factor-beta1 complex. (13/24)

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Ribbing disease: a case report and literature review. (14/24)

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Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFbeta1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. (15/24)

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Fatal cerebellar herniation secondary to Camurati-Englemann's disease. (16/24)

Suboccipital craniotomy and cervical laminectomy were performed in a patient with Camurati-Englemann's disease to relieve symptoms of medullary compression. In spite of surgical decompression, the patient expired on the fourth postoperative day from cerebellar herniation.  (+info)