Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Primary conjunctival amyloidosis presenting as upper lid ectropion
Orbit. 2023 Nov 30:1. doi: 10.1080/01676830.2023.2283178. Online ahead of print.NO ABSTRACTPMID:38032609 | DOI:10.1080/01676830.2023.2283178 (Source: Orbit)
Source: Orbit - November 30, 2023 Category: Opthalmology Authors: Janhavi Desai Md Shahid Alam Source Type: research
Colposcopy-A Valuable Diagnostic Tool for Pregnant Women With Unexplained Vaginal Bleeding
CONCLUSIONS: Colposcopy can be a valuable diagnostic tool for women with unexplained vaginal bleeding in the second or third trimester.PMID:37963328 | DOI:10.1097/LGT.0000000000000783 (Source: Herpes)
Source: Herpes - November 14, 2023 Category: Infectious Diseases Authors: Inshirah Sgayer Maskit Shmueli Lior Lowenstein Maya Frank Wolf Source Type: research
Colposcopy-A Valuable Diagnostic Tool for Pregnant Women With Unexplained Vaginal Bleeding
CONCLUSIONS: Colposcopy can be a valuable diagnostic tool for women with unexplained vaginal bleeding in the second or third trimester.PMID:37963328 | DOI:10.1097/LGT.0000000000000783 (Source: Herpes)
Source: Herpes - November 14, 2023 Category: Infectious Diseases Authors: Inshirah Sgayer Maskit Shmueli Lior Lowenstein Maya Frank Wolf Source Type: research
Clinical Features, Evaluation, and Management of Ophthalmic Complications of Facial Paralysis: A Review
The purpose of this review is to demonstrate the ophthalmic complications of facial nerve palsy, methods of evaluation, and current and future directions for management. The ophthalmic complications of facial paralysis include lagophthalmos, ectropion, exposure keratopathy, ocular synkinesis, and crocodile tears. Evaluation by an ophthalmologist skilled in recognizing and managing complications of facial paralysis soon after initial diagnosis of facial paralysis can help identify and prevent long term complications. (Source: Journal of Plastic, Reconstructive and Aesthetic Surgery)
Source: Journal of Plastic, Reconstructive and Aesthetic Surgery - October 19, 2023 Category: Cosmetic Surgery Authors: Maria Claudia Moncaliano, Peng Ding, Jeffrey M. Goshe, Dane J. Genther, Peter J Ciolek, Patrick J. Byrne Source Type: research
PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serin biosynthesis defect
Eur J Med Genet. 2023 Sep 25:104852. doi: 10.1016/j.ejmg.2023.104852. Online ahead of print.ABSTRACTDefects in L-serine biosynthesis are a group of autosomal recessive diseases resulting in a wide phenotypic spectrum ranging from viable to lethal presentations and caused by variants in the three genes encoding the L-serine biosynthesis enzymes, PHGDH, PSAT1, and PSPH. Neu-Laxova syndrome (NLS) is the fetal form of this group, characterized by multiple congenital anomalies including severe intrauterine growth retardation, cutaneous lesions extending from ichthyosis to severe restrictive dermopathy with ectropion and eclabio...
Source: European Journal of Medical Genetics - September 27, 2023 Category: Genetics & Stem Cells Authors: Silvestre Cuinat Chlo é Quélin Laurent Pasquier Philippe Loget Dominique Aussel Sylvie Odent Annie Laquerri ère Maia Proisy Sylvie Mazoyer Marion Delous Patrick Edery Nicolas Chatron Gaetan Lesca Audrey Putoux Source Type: research
PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serin biosynthesis defect
Eur J Med Genet. 2023 Sep 25:104852. doi: 10.1016/j.ejmg.2023.104852. Online ahead of print.ABSTRACTDefects in L-serine biosynthesis are a group of autosomal recessive diseases resulting in a wide phenotypic spectrum ranging from viable to lethal presentations and caused by variants in the three genes encoding the L-serine biosynthesis enzymes, PHGDH, PSAT1, and PSPH. Neu-Laxova syndrome (NLS) is the fetal form of this group, characterized by multiple congenital anomalies including severe intrauterine growth retardation, cutaneous lesions extending from ichthyosis to severe restrictive dermopathy with ectropion and eclabio...
Source: European Journal of Medical Genetics - September 27, 2023 Category: Genetics & Stem Cells Authors: Silvestre Cuinat Chlo é Quélin Laurent Pasquier Philippe Loget Dominique Aussel Sylvie Odent Annie Laquerri ère Maia Proisy Sylvie Mazoyer Marion Delous Patrick Edery Nicolas Chatron Gaetan Lesca Audrey Putoux Source Type: research
PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect
Eur J Med Genet. 2023 Sep 25;66(11):104852. doi: 10.1016/j.ejmg.2023.104852. Online ahead of print.ABSTRACTDefects in L-serine biosynthesis are a group of autosomal recessive diseases resulting in a wide phenotypic spectrum ranging from viable to lethal presentations and caused by variants in the three genes encoding the L-serine biosynthesis enzymes, PHGDH, PSAT1, and PSPH. Neu-Laxova syndrome (NLS) is the fetal form of this group, characterized by multiple congenital anomalies including severe intrauterine growth retardation, cutaneous lesions extending from ichthyosis to severe restrictive dermopathy with ectropion and ...
Source: European Journal of Medical Genetics - September 27, 2023 Category: Genetics & Stem Cells Authors: Silvestre Cuinat Chlo é Quélin Laurent Pasquier Philippe Loget Dominique Aussel Sylvie Odent Annie Laquerri ère Maia Proisy Sylvie Mazoyer Marion Delous Patrick Edery Nicolas Chatron Gaetan Lesca Audrey Putoux Source Type: research
PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect
Eur J Med Genet. 2023 Sep 25;66(11):104852. doi: 10.1016/j.ejmg.2023.104852. Online ahead of print.ABSTRACTDefects in L-serine biosynthesis are a group of autosomal recessive diseases resulting in a wide phenotypic spectrum ranging from viable to lethal presentations and caused by variants in the three genes encoding the L-serine biosynthesis enzymes, PHGDH, PSAT1, and PSPH. Neu-Laxova syndrome (NLS) is the fetal form of this group, characterized by multiple congenital anomalies including severe intrauterine growth retardation, cutaneous lesions extending from ichthyosis to severe restrictive dermopathy with ectropion and ...
Source: European Journal of Medical Genetics - September 27, 2023 Category: Genetics & Stem Cells Authors: Silvestre Cuinat Chlo é Quélin Laurent Pasquier Philippe Loget Dominique Aussel Sylvie Odent Annie Laquerri ère Maia Proisy Sylvie Mazoyer Marion Delous Patrick Edery Nicolas Chatron Gaetan Lesca Audrey Putoux Source Type: research
