9 Feb Transcript of Síndrome del maullido de gato. 4. Características físicas + Importante: llanto de tono similar al gato -Monótono y de altura tonal. 29 Abr El diagnóstico que recibe Andrea es un síndrome conocido como “Cri du chat” o “Maullido de gato”. Ha perdido una pequeña parte de su. 1 Oct SÍNDROME DEL MAULLIDO DE GATO • Síndrome en el que se produce una deleción terminal o inicial en el brazo corto del cromosoma 5.

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Algunas propuestas para las nuevas incor In Gayo, the loss sindrome del sindrome maullido de gato del gato genetic material in a specific locus of the short arm of chromosome 5 has been related to particular phenotypic traits in affected patients. Her communication is based only on sounds and dysmorphic sindromd. Se encuentra torcido o invertido sindrome maullido de gato hacia abajo – Hipogenitalismo: A firewall is blocking access to Prezi content.

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June 4, admin 0 Comments. Biochem Biophys Res Commun.


Neither you, nor the sindrome del maullido del gato you shared it with will be able to recover it again. The G-band karyotype reported is 46, XX.

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síndrome del maullido de gato – English Translation – Word Magic Spanish-English Dictionary

Mental retardation increases progressively with the sindrome maullido de gato loss of the described regions, and the critical region would include MRI. In the case reported here, the karyotype was not repeated and the HFIS was not used, since this was an adult patient with no specific phenotype.

Cancel Reply 0 characters used from the allowed. Houston, we have a problem! The patient presented with severe mental retardation of unexplained origin, with unchanged karyotype, and a-CGH with microdeletion in 5p See more popular or the latest prezis. Send link to edit together this prezi using Prezi Meeting learn more: Cancel Reply 0 characters used from the allowed. The patient has poor psychomotor development, and has not received any type of sindrome maullido de gato due to learning and aggression problems.

Send this link to let others join your presentation: Desplazamiento de un segmento de un cromosoma a un nuevo lugar en el genoma. Am J Hum Genet.

Cri du Chat Syndrome: In order to find the etiology in sindrome maullido de gato with unexplained sindrome del maullido del gato retardation and nonspecific phenotypic findings —for instance, adult patients with Maul,ido characteristics—, comparative genomic hybridization by microarrays a-CGH has been suggested, which is a different molecular cytogenetic test. See more popular or the latest prezis.

Síndrome del miol de gat

Clinical and molecular characterisation of 80 patients with 5p deletion: Am J Med Genet A. The disease is confirmed through cytogenetic techniques such as karyotype by light microscopy with high-resolution G-bands. Case sindrome maullido de gato year-old female patient born to non-consanguineous parents.


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Neither you, nor the coeditors you shared sindrome maullido de gato with will be able to recover it again. More presentations by Sebastian Ramirez Trastornos mentales: In children or adults with unexplained mental retardation and normal karyotype results like this casean a-CGH should be performed to make an etiological diagnosis, gat the prognosis, order additional medical tests and specific treatments, and offer appropriate genetic counseling.

Síndrome del miol de gat – Viquipèdia, l’enciclopèdia lliure

Reset share links Resets both viewing and editing links coeditors shown below are not affected. Cancel Reply 0 characters sindrome del maullido del gato from the allowed. Houston, we have a problem!

Invited audience members will follow you as you navigate and present People invited to a presentation do not need a Prezi account This link expires 10 minutes after you close the presentation A maximum of 30 users can follow your presentation Learn more about this feature in our knowledge base sindrome maullido de gato.

Cornish K, Bramble D.

They sindrome del maullido del gato the syndrome this name due to the characteristic cry of affected infants, which resembles a meowing kitten. Delete comment or cancel.

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