Speech difficulties in Joubert syndrome

Authors

  • Ghelichi, Leila Speech-Language Pathology Department, School of Rehabilitation Sciences, Iran University of Medical Sciences, Tehran, Iran
  • Khodadoust , Mahdi Kerman Neuroscience Research Center, Kerman University of Medical Sciences, Kerman, Iran.
  • Pourzaki, Mojtaba Toos Clinicof Speech-Language Pathology, Mashhad, Iran
Abstract:

Introduction: "Joubert syndrome" was first introduced in1969. This syndrome is a rare genetic disease with autosomal dominantpattern. Hypotonia, ataxia and motor delay of the disease known as clinical manifestations. In the few reports of this syndrome, mostly functional and structural components studied and radiographic images such as speech and language developmental delay symptoms has been less attention. Some studies report speech features such as sound deletion and distortion, low speech intelligibility, delay in first word and morphology. Few reports of this syndrome have focused on the structural and functional aspects that seen in radiographic images and there has been little attention to growth retardation symptoms such as speech disorders. Speech and language pathologist in dealing with this syndrome requires knowledge of its symptoms and signs in order to be able to determine the treatment priorities and prognosis. The present report describes the syndrome symptoms of the two sisters, 3 and 7 years old. Case reports: A psychiatrist referred Fatima (7 years old) to a private speech-language pathology clinic in Mashhad (Iran). In the first session, it became clear that younger sister (Yasna) has the same syndrome. Two speech-language pathologist evaluated Yasna and Fatima. Fatima speech features include: low quality, low pitch, poor intensity, increasing the overall quality of voice with increasing intensity, maximum phonation time: 5s, mild hypernasality. Speech intelligibility for parents and strangers is70 and 50 percent relatively. Much of the fricatives become explosive and deviation is less in explosive consonants. Fronting is the most common phonological process. Low oral pressure leads to poor production in oral consonants such as/p/and/t/. The results of evaluations in Yasna indicated: speech intelligibility for parents and for the stranger is 70 and 50 percentage, maximum phonation time is7seconds, and thoracic–abdominal breathing pattern. Conversion of fricatives and glides to explosive. Fronting is the most common phonological process Conclusion: Due to the mismatch of speech features of these patients, speech marks of this syndrome seem require further review through Studies with larger sample size

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Joubert syndrome.

Joubert syndrome is an autosomal recessive condition in which there is a variable combination of central nervous system defects with a distinctive congenital retinal dystrophy, ocular motor abnormalities, and respiratory abnormalities in early infancy. The retinal dystrophy has been previously classified as a variant of Leber's congenital amaurosis. We report electrophysiologic and eye movement...

full text

MRI in Joubert Syndrome

The patient was an 8-month-old boy who was the product of a full-term and uncomplicated pregnancy. He had a remarkable family history with the presence of the same clinical course in a cousin, who was not clearly diagnosed as having Joubert Syndrome. He had apnea episodes, truncal ataxia, pendular nystagmus and mentalmotor developmental delay. He had a normal vestibuloocular reflex based on hea...

full text

Lingual Frenectomy in Joubert Syndrome.

AIM Our aim is to present a case of a rare disorder, such as Joubert syndrome (JS) which required oral surgical intervention under general anesthesia at a very young age to help in achieving normal developmental milestones. BACKGROUND Ciliopathies are an emerging class of diseases of which JS is a significant member. There have been very few cases of JS with its distinguishing features which ...

full text

Neurobehavioral development in Joubert syndrome.

Research on children with Joubert syndrome has focused on brain structural abnormalities and associated clinical symptoms. The degree of developmental delay has not been objectively reported. We investigated the neurobehavioral development of children with Joubert syndrome through neurobehavioral assessment in the largest sample to date. Thirty-two parents of children with Joubert syndrome comp...

full text

Prenatal diagnosis of Joubert syndrome

Introduction: Joubert syndrome (JS) is a rare autosomal recessive inherited disease belonging to ciliopathy with the causative mutation of genes. Except for X-linked inheritance, the high recurrence rate of a family is about 25%. After birth, it may cause a series of neurological symptoms, even with retina, kidney, liver, and other organ abnormalities, which is defined as Joubert syndrome and r...

full text

Speech Difficulties in Childhood

and encec* worker in the field of speech therapy, she is a most humane, sensitive te(jjoysn^erstanding person. Her style of writing is clear and simple, yet never tj^ first chapter deals with normal development of speech?not only giving 8es and norms in the form of number of words and length of sentences used f0r fxPlaining clearly how speech, both heard and spoken, comes to have meaning eoiotn...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 21  issue 2

pages  387- 390

publication date 2019-04

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

No Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023