apert's syndrome

  • 41Childhood tumor syndrome — is a condition characterized by axillary freckling, neurofibromas and/or CNS gliomas.[1] See also Apert syndrome List of cutaneous conditions References ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2 Volume Set …

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  • 42Crouzon syndrome — craniofacial dysostosis a genetic disorder characterized by premature fusion of the skull sutures, leading to distortion in the shape of the head. It is a generalized form of craniosynostosis, with a wide skull, high forehead, widely spaced eyes… …

    The new mediacal dictionary

  • 43Craniosynostosis — Classification and external resources Child with premature closure (craniosynostosis) of the lambdoid suture. Notice the swelling on the right side of the head ICD 10 …

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  • 44Синдром Аперта — Синдром Апера Дети с синдромом Апера МКБ 10 Q …

    Википедия

  • 45Webbed toes — Infobox Disease Name = PAGENAME Caption = Human foot with partial simple syndactyly. DiseasesDB = ICD10 = ICD10|Q|70|3|q|65 ICD9 = ICD9|755.13 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Webbed toes is the common name… …

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  • 46Craniofacial surgery — is a surgical subspecialty of maxillofacial surgery, plastic surgery, and ENT that deals with congenital and acquired deformities of the skull, face, and jaws. Although craniofacial treatment often involves manipulation of bone, craniofacial… …

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  • 47Donald Wood-Smith — Donald Wood Smith, MD, FACS, FRCS is a Professor of Clinical Surgery at Columbia University College of Physicians and Surgeons, and an Attending Surgeon at NewYork Presbyterian Hospital/Columbia University Medical Center. He is also Chairman of… …

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  • 48acrocephalosyndactyly type I — Apert syndrome …

    Medical dictionary

  • 49Список наследственных заболеваний — Список генетических заболеваний Основные статьи: наследственные заболевания, Наследственные болезни обмена веществ, Ферментопатия. В большинстве случаев приведен также код, указывающий на тип мутации и связанные с ней хромосомы. См. также система …

    Википедия

  • 50Hearing loss with craniofacial syndromes — is a common occurrence. Many of these multianomaly disorders involve structural malformations of the outer or middle ear, making a significant hearing loss highly likely. Treacher Collins syndrome Individuals with Treacher Collins syndrome often… …

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