000			05378cam a22006138i 4500
001			on1000150685
003			OCoLC
005			20221128213402.0
006			m d
007			cr cn|||||||||
008			170807s2018 nyua obf 001 0 eng
010			_a 2017037367
040			_aDLC _beng _erda _epn _cDLC _dOCLCO _dOCLCQ _dN$T _dOCLCA _dKOS _dOCLCO _dSAV _dOCLCO _dOCLCF _dOCLCO _dYDX _dOCLCA _dLOA _dOCL _dCOCUF _dUSU _dCUX
019			_a1051040759
020			_a9781626232945 _q(electronic bk.)
020			_a1626232946 _q(electronic bk.)
020			_z9781626232938
020			_z1626232938
035			_a1664770 _b(N$T)
035			_a(OCoLC)1000150685 _z(OCoLC)1051040759
042			_apcc
060	1	0	_aWW 140
060		4	_aWW 39
072		7	_aMED _x085000 _2bisacsh
049			_aMAIN
100	1		_aLevin, Alex V., _d1957- _eauthor.
245	1	4	_aThe Wills Eye handbook of ocular genetics _c _h[E-Book]
246	3		_aHandbook of ocular genetics
263			_a1804
264		1	_aNew York : _bThieme, _c[2018]
300			_a1 online resource : _billustrations
336			_atext _btxt _2rdacontent
336			_astill image _bsti _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
588			_aDescription based on print version record
504			_aIncludes bibliographical references and index
505	0		_aBasic Genetics -- Inheritance Patterns -- Genetic Testing -- Ethical Issues -- Corneal Dystrophies - Aniridia -- Peters Anomaly -- Axenfeld-Rieger Syndrome -- Primary Congenital Glaucoma and Juvenile Open Angle Glaucoma -- Childhood Cataract - Microphthalmia -- Marfan Syndrome and Other Causes of Ectopia Lentis -- Familial Exudative Vitreoretinopathy -- Stickler Syndrome -- VCAN Vitreoretinopathies (Erosive Vitreoretinopathy and Wagner Syndrome) -- Incontinentia Pigmenti -- Retinitis Pigmentosa -- Usher Syndrome -- Bardet-Biedl Syndrome -- Cone-Rod Dystrophy - Choroideremia -- Enhanced S-Cone Syndrome and Other NR2E3-Related Retinal Dystrophies -- Stargardt Disease and Other ABCA4 Retinopathies -- Best Vitelliform Macular Dystrophy (Best Disease) -- Leber Congenital Amaurosis - Achromatopsia -- Congenital Stationary Night Blindness -- Juvenile X-Linked Retinoschisis - Retinoblastoma -- Optic Nerve Hypoplasia -- Leber Hereditary Optic Neuropathy -- Complex Ocular Disorders - Albinism.
520			_a"Many serious, potentially blinding eye disorders have a genetic basis. Currently, there are relatively few ocular geneticists in the world, yet inherited eye disease is one of the leading causes of blindness worldwide. Significant strides have been made in gene identification and acquisition of knowledge on the underlying mechanisms of hereditary eye disease. The field of ocular genetics is becoming an increasingly relevant part of ophthalmologists'purview. This has resulted in a dire need for a comprehensive textbook ophthalmologists and other professionals who work with patients with genetic disorders can utilize to gain a better understanding of inherited eye disorders.The Wills Eye Handbook of Ocular Genetics, by Alex Levin, Mario Zanolli, and Jenina Capasso of Wills Eye Hospital, is a practical, reader-friendly guide on the diagnosis and management of ophthalmic genetic conditions. Every chapter begins with a disease overview, followed by relevant modern genetic concepts, pathways to attaining the correct diagnosis, and pitfalls and pearls gleaned from years of hands-on expertise. At the end of each chapter, questions and answers enable readers to test their knowledge in real-life scenarios they might face in everyday practice. The ultimate goal of this clinically robust handbook is to facilitate optimal patient management and outcomes.Key FeaturesFundamentals, including basic genetics, inheritance patterns, genetic testing, and ethical issuesPatient-centered genetic counseling issues such as reproduction, dealing with emotional reactions, prognosis, and future optionsAnterior segment disorders - from corneal dystrophies and aniridia - to childhood cataract and microphthalmiaA broad spectrum of vitreoretinopathies and retinal diseases including incontinentia pigmenti, retinitis pigmentosa, Bardet-Biedl syndrome, choroideremia, Stargardt disease, achromatopsia, and juvenile X-linked retinoschisisThis textbook is essential reading for practitioners at all levels and in all subspecialties including ophthalmology and genetics. They will find it an excellent resource for navigating the complexities of genetic eye disease."--Publisher.
590			_aMaster record variable field(s) change: 650
650		0	_aEye _xDiseases _xGenetics _vHandbooks, manuals, etc.
650		0	_aEye _xDiseases.
650		0	_aGenetic diseases and disorders.
650		2	_aEye Diseases, Hereditary _xgenetics.
650		2	_aEye Diseases, Hereditary _xtherapy.
700	1		_aZanolli, Mario, _eauthor.
700	1		_aCapasso, Jenina, _eauthor.
710	2		_aWills Eye Hospital (Philadelphia, Pa.)
856	4	0	_uhttps://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=1664770 _yKingston Hospital NHS Foundation Trust OpenAthens account holders click here for access
938			_aEBSCOhost _bEBSC _n1664770
938			_aYBP Library Services _bYANK _n15064137
942			_n0
994			_a92 _bN$T
999			_c92953 _d92953