نتایج جستجو برای: microphthalmia

تعداد نتایج: 1639  

Journal: :International Journal of Epidemiology 1996

Journal: :British Journal of Ophthalmology 1921

Journal: :American journal of human genetics 2011
Ippei Okada Haruka Hamanoue Koji Terada Takaya Tohma Andre Megarbane Eliane Chouery Joelle Abou-Ghoch Nadine Jalkh Ozgur Cogulu Ferda Ozkinay Kyoji Horie Junji Takeda Tatsuya Furuichi Shiro Ikegawa Kiyomi Nishiyama Satoko Miyatake Akira Nishimura Takeshi Mizuguchi Norio Niikawa Fumiki Hirahara Tadashi Kaname Koh-Ichiro Yoshiura Yoshinori Tsurusaki Hiroshi Doi Noriko Miyake Takahisa Furukawa Naomichi Matsumoto Hirotomo Saitsu

Microphthalmia with limb anomalies (MLA) is a rare autosomal-recessive disorder, presenting with anophthalmia or microphthalmia and hand and/or foot malformation. We mapped the MLA locus to 14q24 and successfully identified three homozygous (one nonsense and two splice site) mutations in the SPARC (secreted protein acidic and rich in cysteine)-related modular calcium binding 1 (SMOC1) in three ...

2008
Panigrahi Inusha Kulkarni Ketan Prasad

Williams MS, et al. CHARGE association: An update and review for the primary pediatrician. Clin Pediatr (Phila) 1998;37:159-73. 6. Amiel J, Attiee-Bitach T, Marianowski R. Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome. Am J Med Genet 2001;99:124-7. 7. Al Frayh AR, Haque KN. Anophthalmia, microcephaly, hypotonia, hypogonadism, failure to thrive and developme...

2012
Eunjung Moon Ae-Jung Kim Sun Yeou Kim

Sarsasapogenin (SAR) is a steroidal sapogenin that is used as starting material for the industrial synthesis of steroids. It has various pharmacological benefits, such as antitumor and antidepressant activities. Since its effect on melanin biosynthesis has not been reported, we used murine melanocyte melan-a cells to investigate whether SAR influences melanogenesis. In this study, SAR significa...

Journal: :Clinical genetics 2008
L Lequeux M Rio A Vigouroux M Titeux H Etchevers F Malecaze N Chassaing P Calvas

Microphthalmia and anophthalmia are at the severe end of the spectrum of abnormalities in ocular development. Mutations in several genes have been involved in syndromic and non-syndromic anophthalmia. Previously, RAX recessive mutations were implicated in a single patient with right anophthalmia, left microphthalmia and sclerocornea. In this study, we report the findings of novel compound heter...

Journal: :Journal of medical genetics 1992
C T Schrander-Stumpel C E de Die-Smulders R C Hennekam J P Fryns P X Bouckaert O F Brouwer J J da Costa E J Lommen P D Maaswinkel-Mooy

We report on three Dutch children with a clinical diagnosis of oculoauriculovertebral spectrum (OAVS) and hydrocephalus. The clinical features are compared to 15 published cases of OAVS and hydrocephalus. Several other cerebral abnormalities were present in the whole group. About half of the cases had cleft lip/palate, anophthalmia/microphthalmia, or a cardiac defect. Mental retardation was fou...

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