متلازمة أبرت:Apert Syndrome

> السؤال:
لدي ابنة عمرها سنتين واربعة اشهر لديها تشوه خلقي نادروهو عبارة عن خلل في كروموزم العظام واسم المرض ابرت ساندروم واريد معرفة تطورات المرض وكيفية التعامل معه وهل هو انواع وهل يختلف من طفل لاخر وما مدى قابلية الطفل المصاب للتعلم والمعرفة علما بان ابنتي تعمل مثل اقرانها ولكن بفارق السن تقريبا اقل من سنة ....ولكم جزيل الشكر

ام البراء , المملكة

> الجواب:

متلازمة أبرت:Apert Syndrome حالة وراثية تنتقل كسمة جينية سائدة ويتميز الطفل صغر حجم جمجمته ويصاحبها إعاقة عقلية بدراجات متفاوتة. لا يتوفر لدينا حاليا شرح كامل عن الحالة يمكنك الاستفادة من المقالة التالية Apert Syndrome is a genetic defect and falls under the broad classification of craniofacial/limb anomalies. It can be inherited from a parent who has Apert, or may be a fresh mutation. It occurs in approximately 1 per 160,000 to 200,000 live births. Apert syndrome is primarily characterized by specific malformations of the skull, midface, hands, and feet. The skull is prematurely fused and unable to grow normally; the midface (that area of the face from the middle of the eye socket to the upper jaw) appears retruded or sunken; and the fingers and toes are fused together in varying degrees. Apert syndrome is named for the French physician who first described it, E. Apert, in 1906. In a normal child, the skull is made up of several "plates" which remain loosely connected to one another, gradually growing together to form the adult skull. The Apert child's skull, by contrast, has a premature fusion of these plates, restricting brain growth, and causing increased pressure in the brain as it grows. This is known as craniosynostosis. Early surgery relieves the pressures by allowing the plates to be detached from one another. During this early surgery some "cranial remodeling" may be done to give the child a more normal appearance. The "retrusion" or hypoplasia of the midface is what could be described as a concave or dished in profile. As the skull grows, the upper and lower thirds of the face tend to grow at normal rates, but the middle third of the face grows slower, resulting in a more pronounced retrusion over time. A surgical procedure known as the LeFort III is used to correct this condition. The procedure is usually done after substantial growth is complete (preadolescence) and may be repeated as necessary. The LeFort procedure involves detaching the facial bones from mid eye to upper jaw and spacing this area out with bone grafts so that a proper alignment is made. In the last few years, some surgeons have come to prefer the Rigid External Distraction (RED) system or internally placed distractors, instead of or in conjunction with, traditional craniofacial surgery. The fusion of the fingers and toes along with the craniofacial problems mentioned above is what really separates Apert from other similar syndromes. This condition is called syndactyly. It always involves fusion of the soft tissues of the first, middle, and ring fingers, and often there is fusion of the bones themselves. Joint mobility is usually nonexistent past the first joint. The thumb may be fused into the hand, or may be free. Surgery is used to separate the fingers to obtain the highest degree of functionality, and may or may not ultimately result in five digits on each hand. It varies according to the degree of malformation. The feet and toes are affected similarly, but surgery is usually only recommended in cases where the ability to walk would be impaired. Ideally, treatment of Apert begins at birth with the proper diagnosis, identification of the child's individual needs, and the proper facilities to administer what is needed. A multidisciplinary approach is used by physicians in the best arrangements. A craniofacial anomalies team may consist of a craniofacial surgeon, neurosurgeon, ENT, audiologist, speech pathologist, oral surgeon, psychologist, ophthalmologist, and an orthodontist. The team approach is used by these physicians to determine the best collaborative corrective plan for the deficiencies of the child.