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LAURENCE MOON BARDET BIEDL
SYNDROME- CASE REPORT AND
REVIEW OF LITERATURE
DR. AZEEMODDIN Y. MASHAYAK
DR. H. T. KARAD ; DR. T. R. GITTE ; DR. SUJATA AGRAWAL;
DR. SOURABH KARAD
ABSTRACT:
Laurence Moon Bardet Biedl syndrome is an autosomal recessive
genetic disorder with variable expressivity and a wide range of clinical
variability observed both within and between families. It includes
Laurence Moon syndrome with features of Retinitis pigmentosa(Rod-
cone dystrophy), mental retardation, hypogenitalism and spastic paresis
and Bardet Biedl syndrome as Retinitis pigmentosa, obesity, postaxial
polydactyly, learning disabilities and hypogenitalism in males. We report
a typical case of Laurence Moon Bardet Biedl syndrome in a male
showing all ocular features, most of the general features and a typical
family history.There is a typical early onset of blindness in this case.
Keywords: Retinitis pigmentosa, polydactyly, mental retardation,
hypogenitalism, obesity, consanguinous marriage.
CASE REPORT
Here is a case of 19 old male who came to our OPD , Ophthalmology
department, YCRH MIMSR medical college; latur; with complaints of night
blindness, jerky eye movements since childhood which progressed gradually
over years.He is born of consanguinous marriage, had developmental delay
and mentally retarded. The other male sibling and parents were normal but
there is family history of similar presentation in one of their relatives . Systemic
examination revealed obesity , polydactyly (hexadactyly) and syndactyly in both
upper and lower limbs, ataxic gait and hypogonadism. Ophthalmic examination
revealed only perception of light in both eyes with nystagmus. On slit lamp
examinatioin there is Posterior subcapsular cataract in both the eyes. Fundus
examination revealed pale, waxy optic disc with attenuation of arterioles and
bony corpuscular pigment seen at periphery giving the impression of Primary
typical Retinitis pigmentosa with consecutive optic atrophy .
DISCUSSION
Laurence Moon Biedl Bardet syndrome was first defined by Bardet in 1922 as an
autosomal recessive disorder characterized by structural and functional
abnormalities of organs and tissues with diverse embryonic derivation. The five
cardinal features of syndrome include – polydactyly , pigmentary retinopathy ,
obesity , mental retardation and hypogonadism . Other systemic features include
short stature , congenital heart block , deafness and neurological disorders .
Laurence Moon Biedl Bardet syndrome is a rare genetic disorder. Biedl in 1922
added mental deficiency and genital hypoplasia to this syndrome . In 1925 Solis-
Cohen and Weiss connected to this syndrome the four patients in one family
described by Laurence and Moon in 1966. Solis- Cohen and Weiss coined the
name Laurence Moon Biedl syndrome. The cases reported by Laurence and Moon
were reevaluated and reported by Hutchinson , the members were found to have a
disease characterized by typical pigmentary retinopathy , mental retardation, arrest
of sexual development and progressive weakness leading to paraplegia.
CONCLUSION
We report a typical case of laurence moon bardet biedl syndrome
in a male of 19 years old with significant family history. He
presented with an early onset blindness and all ocular features
like retinitis pigmentosa, optic atrophy, posterior subcapsular
cataract and nystagmus. He also showed characteristic general
features of obesity, polydactyly, syndactyly. He also had mental
retardation and developmental delay.
REFERENCES
[1] Fauci Braunwald Casper Hauser Coyo Jameson Localso, 17th edition,
Harrison’s Principles of Internal Medicine Volume-II, Part 15:Endocrinology and
Metabolism, Section-I- Endocrinology, 333- Disorders of Anterior Pituitary and
Hypothalamus pg-2198.
[2] Jack J Kanski and Brad Bowling , 7th edition, Clinical Ophthalmology, 15th
chapter- Hereditary Fundus dystrophies-Generalized photoreceptor
dystrophies.
[3] Fauci Braunwald Casper Hauser Coyo Jameson Localso, 17th edition,
Harrison’s Principles of Internal Medicine Volume-II, Part 15:Endocrinology and
Metabolism, Section-I- Endocrinology, 340-Disorders of testis and male
reproductive system Congenital disorders associated with gonadotropin
deficiency , pg 2316.
[4] Putoux A, Attie-Bitach T, Martinovic J, et al; Phenotypic variability of Bardet-
Biedl syndrome: focusing on the kidney. Pediatr Nephrol. 2012 Jan;27(1):7-15.
Epub 2011 Jan 19.
[5] Bardet-Biedl Syndrome, Online Mendelian Inheritance in Man (OMIM).
[6] Pereiro I, Valverde D, Pineiro-Gallego T, et al; New mutations in BBS genes
in small consanguineous families with Bardet-Biedl Mol Vis. 2010 Feb 1;16:137-
43.

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Laurence Moon Bardet Biedl Syndrome- Case Report And Review Of Literature

  • 1. LAURENCE MOON BARDET BIEDL SYNDROME- CASE REPORT AND REVIEW OF LITERATURE DR. AZEEMODDIN Y. MASHAYAK DR. H. T. KARAD ; DR. T. R. GITTE ; DR. SUJATA AGRAWAL; DR. SOURABH KARAD
  • 2. ABSTRACT: Laurence Moon Bardet Biedl syndrome is an autosomal recessive genetic disorder with variable expressivity and a wide range of clinical variability observed both within and between families. It includes Laurence Moon syndrome with features of Retinitis pigmentosa(Rod- cone dystrophy), mental retardation, hypogenitalism and spastic paresis and Bardet Biedl syndrome as Retinitis pigmentosa, obesity, postaxial polydactyly, learning disabilities and hypogenitalism in males. We report a typical case of Laurence Moon Bardet Biedl syndrome in a male showing all ocular features, most of the general features and a typical family history.There is a typical early onset of blindness in this case. Keywords: Retinitis pigmentosa, polydactyly, mental retardation, hypogenitalism, obesity, consanguinous marriage.
  • 3. CASE REPORT Here is a case of 19 old male who came to our OPD , Ophthalmology department, YCRH MIMSR medical college; latur; with complaints of night blindness, jerky eye movements since childhood which progressed gradually over years.He is born of consanguinous marriage, had developmental delay and mentally retarded. The other male sibling and parents were normal but there is family history of similar presentation in one of their relatives . Systemic examination revealed obesity , polydactyly (hexadactyly) and syndactyly in both upper and lower limbs, ataxic gait and hypogonadism. Ophthalmic examination revealed only perception of light in both eyes with nystagmus. On slit lamp examinatioin there is Posterior subcapsular cataract in both the eyes. Fundus examination revealed pale, waxy optic disc with attenuation of arterioles and bony corpuscular pigment seen at periphery giving the impression of Primary typical Retinitis pigmentosa with consecutive optic atrophy .
  • 4.
  • 5. DISCUSSION Laurence Moon Biedl Bardet syndrome was first defined by Bardet in 1922 as an autosomal recessive disorder characterized by structural and functional abnormalities of organs and tissues with diverse embryonic derivation. The five cardinal features of syndrome include – polydactyly , pigmentary retinopathy , obesity , mental retardation and hypogonadism . Other systemic features include short stature , congenital heart block , deafness and neurological disorders . Laurence Moon Biedl Bardet syndrome is a rare genetic disorder. Biedl in 1922 added mental deficiency and genital hypoplasia to this syndrome . In 1925 Solis- Cohen and Weiss connected to this syndrome the four patients in one family described by Laurence and Moon in 1966. Solis- Cohen and Weiss coined the name Laurence Moon Biedl syndrome. The cases reported by Laurence and Moon were reevaluated and reported by Hutchinson , the members were found to have a disease characterized by typical pigmentary retinopathy , mental retardation, arrest of sexual development and progressive weakness leading to paraplegia.
  • 6. CONCLUSION We report a typical case of laurence moon bardet biedl syndrome in a male of 19 years old with significant family history. He presented with an early onset blindness and all ocular features like retinitis pigmentosa, optic atrophy, posterior subcapsular cataract and nystagmus. He also showed characteristic general features of obesity, polydactyly, syndactyly. He also had mental retardation and developmental delay.
  • 7. REFERENCES [1] Fauci Braunwald Casper Hauser Coyo Jameson Localso, 17th edition, Harrison’s Principles of Internal Medicine Volume-II, Part 15:Endocrinology and Metabolism, Section-I- Endocrinology, 333- Disorders of Anterior Pituitary and Hypothalamus pg-2198. [2] Jack J Kanski and Brad Bowling , 7th edition, Clinical Ophthalmology, 15th chapter- Hereditary Fundus dystrophies-Generalized photoreceptor dystrophies. [3] Fauci Braunwald Casper Hauser Coyo Jameson Localso, 17th edition, Harrison’s Principles of Internal Medicine Volume-II, Part 15:Endocrinology and Metabolism, Section-I- Endocrinology, 340-Disorders of testis and male reproductive system Congenital disorders associated with gonadotropin deficiency , pg 2316. [4] Putoux A, Attie-Bitach T, Martinovic J, et al; Phenotypic variability of Bardet- Biedl syndrome: focusing on the kidney. Pediatr Nephrol. 2012 Jan;27(1):7-15. Epub 2011 Jan 19. [5] Bardet-Biedl Syndrome, Online Mendelian Inheritance in Man (OMIM). [6] Pereiro I, Valverde D, Pineiro-Gallego T, et al; New mutations in BBS genes in small consanguineous families with Bardet-Biedl Mol Vis. 2010 Feb 1;16:137- 43.