Top 20 apert syndrome: quality of life in 2023
Below are the best information and knowledge on the subject apert syndrome: quality of life compiled and compiled by our own team thoitrangredep:
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1. Apert Syndrome: Symptoms, Causes, Diagnosis, Treatment, Prognosis
Author: www.webmd.com
Date Submitted: 04/02/2021 10:17 AM
Average star voting: 5 ⭐ ( 70874 reviews)
Summary: WebMD describes Apert syndrome, a genetic disorder that can cause abnormalities in the formation of the head and other parts of the body.
Match with the search results: Those with Apert syndrome who survive past childhood and don’t have heart problems likely have a …. read more
2. Apert Syndrome: Quality of Life and Challenges of a Manageme… : Journal of Craniofacial Surgery
Author: pubmed.ncbi.nlm.nih.gov
Date Submitted: 11/09/2021 09:10 PM
Average star voting: 5 ⭐ ( 16907 reviews)
Summary:
Match with the search results: The quality of life for patients born with Apert syndrome may be strongly affected by the limitations that this syndrome imposes. The aims of this study were to ……. read more
3. Assessment of long-term quality of life in patients with syndromic craniosynostosis
Author: journals.lww.com
Date Submitted: 08/09/2022 10:58 PM
Average star voting: 4 ⭐ ( 54331 reviews)
Summary:
Match with the search results: The quality of life for patients born with Apert syndrome may be strongly affected by the limitations that this syndrome imposes. The aims of this study ……. read more
4. Health-related problems and quality of life in patients with syndromic and complex craniosynostosis | SpringerLink
Author: www.sciencedirect.com
Date Submitted: 09/13/2022 03:15 AM
Average star voting: 3 ⭐ ( 14940 reviews)
Summary: We conducted this study to gauge the health-related problems, quality of life and the performance of the Health Utility Index Mark 3 (HUI-3) in patients wi
Match with the search results: Apert syndrome patients were found to have difficulty in understanding, communication, and self-care because of their mental retardation and hand and foot ……. read more
5. Apert Syndrome: What Is It, Symptoms, Diagnosis & Treatment
Author: www.jprasurg.com
Date Submitted: 09/15/2022 01:03 AM
Average star voting: 3 ⭐ ( 85837 reviews)
Summary: Apert syndrome is a rare genetic condition that causes a baby’s skull, face, feet and hands to form atypically when the skull joints close too soon.
Match with the search results: Apert syndrome patients were found to have difficulty in understanding, communication, and self-care because of their mental retardation and hand and foot ……. read more
6. Revolutionary New Surgery for Complex Craniosynostosis
Author: link.springer.com
Date Submitted: 01/23/2020 02:50 AM
Average star voting: 4 ⭐ ( 26207 reviews)
Summary: A revolutionary new surgery changes the picture for children with Apert syndrome.
Match with the search results: Ambulation and dexterity problems were seen in Apert, Crouzon, Saethre–Chotzen and complex craniosynostosis. Only patients with Apert syndrome ……. read more
7. Apert Syndrome: Symptoms, Causes, Diagnosis, and Treatment
Author: www.researchgate.net
Date Submitted: 11/26/2021 02:23 AM
Average star voting: 3 ⭐ ( 74647 reviews)
Summary: Apert syndrome is a rare disorder that occurs due to a genetic mutation in the FGFR2 gene. Learn more about symptoms, causes, and quality of life.
Match with the search results: The quality of life for patients born with Apert syndrome may be strongly affected by the limitations that this syndrome imposes. The aims of this study ……. read more
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8. Apert Syndrome | Children’s Hospital Colorado
Author: my.clevelandclinic.org
Date Submitted: 03/31/2020 01:28 AM
Average star voting: 4 ⭐ ( 25491 reviews)
Summary: Learn about the rare Apert syndrome, aka Acrocephalosyndactyly, how it is diagnosed & how the experts at Children’s Colorado can help with treatment.
Match with the search results: Apert syndrome is a genetic condition that may require several surgeries to alleviate symptoms but ultimately leads to your child living a full ……. read more
9. Apert Syndrome | Boston Children’s Hospital
Author: www.seattlechildrens.org
Date Submitted: 01/22/2021 02:33 PM
Average star voting: 4 ⭐ ( 71355 reviews)
Summary:
Apert syndrome, aka acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones. Learn more from Boston Children’s.
Match with the search results: Apert syndrome is a rare and extreme form of craniosynostosis, where one or more of the special … but I had to do this to improve his quality of life.”….. read more
10. A 37-year-old Nigerian woman with Apert syndrome – medical and psychosocial perspectives: a case report – Journal of Medical Case Reports
Author: www.verywellhealth.com
Date Submitted: 08/16/2021 03:33 PM
Average star voting: 3 ⭐ ( 16676 reviews)
Summary: Apert syndrome is a rare genetic disease that presents a diagnostic dilemma because of its similarity with other craniosynostosis syndromes. Currently, there is paucity of reports about adult patients in African medical literature. Therefore, this case report highlights medical and psychosocial problems associated with the disease in an adult woman who is resident in a resource-constrained setting. Our patient is a 37-year-old African woman. She had abnormal characteristics of the skull, face, and extremities that were detected at birth. She is clinically stable but moderately depressed as an adult. Mutation in fibroblast growth factor receptor 2 (Ser252Trp) was positive. Her physical deformities and the laboratory findings confirmed the diagnosis of Apert syndrome. She missed opportunities for vital interventions to limit the physical and psychosocial effects of the disease, especially during early growth and developmental period, mainly due to the inadequacy of the institutions offering medical and psychosocial support. As a child she did not complete formal education or acquire vocational skills even though intellectual disability was never established. During adulthood she became socially deprived owing to her physical features and educational handicap. Her lifelong dependency is an unfortunate social consequence starting with developmental challenges encountered during childhood and worsened by adult social maladjustment. Our patient does not have medically life-threatening features but was depressed. We recommend strengthening of institutions for early medical intervention and lifetime psychosocial support to limit physical and psychosocial effects of Apert syndrome among adult survivors in resource-limited settings.
Match with the search results: 1 Common traits in people with Apert syndrome include prematurely fused bones of the skull, fusion of some fingers and toes, among others….. read more
11. What is Apert Syndrome?
Author: www.childrenscolorado.org
Date Submitted: 03/08/2022 04:09 AM
Average star voting: 3 ⭐ ( 98656 reviews)
Summary: Apert syndrome (AS) is a genetic disorder that involves deformities in the skull, face, and limbs.
Match with the search results: Those with Apert syndrome who survive past childhood and don’t have heart problems likely have a …. read more
12. Apert syndrome
Author: www.childrenshospital.org
Date Submitted: 01/19/2019 05:59 AM
Average star voting: 3 ⭐ ( 55825 reviews)
Summary: Apert syndrome is a rare condition that causes an abnormally shaped skull and fused fingers and toes. Other body parts and organs are also affected. Surgery and other treatments can, however, help development.
Match with the search results: The quality of life for patients born with Apert syndrome may be strongly affected by the limitations that this syndrome imposes. The aims of this study were to ……. read more
13. Apert Syndrome – Pediatric Cleft and Craniofacial Center – Golisano Children’s Hospital – University of Rochester Medical Center
Author: europepmc.org
Date Submitted: 06/28/2021 03:24 AM
Average star voting: 4 ⭐ ( 19721 reviews)
Summary:
Match with the search results: The quality of life for patients born with Apert syndrome may be strongly affected by the limitations that this syndrome imposes. The aims of this study ……. read more
14. Pediatric Apert Syndrome
Author: jmedicalcasereports.biomedcentral.com
Date Submitted: 04/06/2021 04:45 AM
Average star voting: 3 ⭐ ( 18900 reviews)
Summary: Apert Syndrome can affect children’s intelligence in different ways. Learn about symptoms, diagnosis, and treatment in and around Dallas from Children’s Health.
Match with the search results: Apert syndrome patients were found to have difficulty in understanding, communication, and self-care because of their mental retardation and hand and foot ……. read more
15. Apert syndrome: MedlinePlus Genetics
Author: www.news-medical.net
Date Submitted: 11/06/2021 09:12 AM
Average star voting: 3 ⭐ ( 12625 reviews)
Summary: Apert syndrome is a genetic disorder characterized by skeletal abnormalities. Explore symptoms, inheritance, genetics of this condition.
Match with the search results: Apert syndrome patients were found to have difficulty in understanding, communication, and self-care because of their mental retardation and hand and foot ……. read more
16. Shine a Light
Author: www.healthdirect.gov.au
Date Submitted: 03/23/2022 07:31 PM
Average star voting: 4 ⭐ ( 58354 reviews)
Summary: University of Hertfordshire
Match with the search results: Ambulation and dexterity problems were seen in Apert, Crouzon, Saethre–Chotzen and complex craniosynostosis. Only patients with Apert syndrome ……. read more
17. Apert Syndrome
Author: www.urmc.rochester.edu
Date Submitted: 12/15/2020 07:49 AM
Average star voting: 5 ⭐ ( 45209 reviews)
Summary: Apert syndrome is a genetic condition that affects the skull, face, hands and feet. Signs of Apert syndrome include craniosynostosis, midface deficiency, hypertelorbitism and syndactyly. The Center for Complex Craniofacial Disorders at Nationwide Children’s expertly treats children with Apert syndrome.
Match with the search results: The quality of life for patients born with Apert syndrome may be strongly affected by the limitations that this syndrome imposes. The aims of this study ……. read more
18. Apert Syndrome: Practice Essentials, Pathophysiology, Epidemiology
Author: www.childrens.com
Date Submitted: 06/16/2022 10:46 AM
Average star voting: 4 ⭐ ( 54326 reviews)
Summary: Apert syndrome is named for the French physician who described the syndrome acrocephalosyndactylia in 1906. Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and severe symmetrical syndactyly (cutaneous and bony fusion) of the hands and feet.
Match with the search results: Apert syndrome is a genetic condition that may require several surgeries to alleviate symptoms but ultimately leads to your child living a full ……. read more
19. Apert Syndrome Lawyer NY | NJ Apert Syndrome Medical Malpractice Attorneys
Author: publications.aston.ac.uk
Date Submitted: 10/08/2019 03:32 AM
Average star voting: 4 ⭐ ( 40487 reviews)
Summary: Our medical and pediatric malpractice attorneys represent victims in cases involving Apert Syndrome and Craniosynostosis in New York, New Jersey, and the U.S.
Match with the search results: Apert syndrome is a rare and extreme form of craniosynostosis, where one or more of the special … but I had to do this to improve his quality of life.”….. read more
20. Apert Syndrome
Author: medlineplus.gov
Date Submitted: 04/22/2021 05:00 PM
Average star voting: 5 ⭐ ( 98356 reviews)
Summary: Apert syndrome is a rare genetic condition that is apparent at birth. People with Apert syndrome can have malformations of the skull, face and hands.
Match with the search results: 1 Common traits in people with Apert syndrome include prematurely fused bones of the skull, fusion of some fingers and toes, among others….. read more
