The document lists various genetic syndromes and their associated symptoms, organized into sections covering different body systems and types of symptoms. It discusses several syndromes involving retinal issues like retinitis pigmentosa, neurological issues like ataxia and mental retardation, deafness, dwarfism, obesity, genital abnormalities, delayed puberty, and increased infection risk. Each syndrome is concisely summarized along with its key symptoms.

1. RETINITIS
PIGMENTOSA
HYPOGONADISM
MENTAL
RETARDATION
OBESITY
POLYDACTYLY
LAURENCE-
MOON-BIEDL
SYNDROME
MENTAL
RETARDATION
INFANTILE
DEAFNESS
DWARFISM
NYSTAGMUS
ATAXIA
COCKAYNE
SYNDROME
PERIFERAL
NEUROPATHY
CEREBELLAR
ATAXIA
REFSUM
SYNDROME
LABYRINTHINE
DEAFNESS
USHER
SYNDROME
VESTIBULO-
CEREBELLAR
ATAXIA
CONGENITAL
DEAFNESS
MENTAL
DEFICIENCY
HALLGREN
SYNDROME
BY- MAYUR PATEL

2. PORTWINE STAIN
JACKSONIAN EPILEPSY
(IPSILATERAL CEREBRAL
HEMANGIOMA)
MENTAL RETARDATION
GLUCOMA
BUPHTHALMOS
STURGE-WEBER
HEMANGIOMA OF….
GIT
URINARY TRACT
LIVER
SPLEEN
BRAIN
OSLER RENDU WEBER
OSTEODYSTROPHY OF
EXTREMITIES
AV FISTULA
KLIPPEL TRENAUNY WEBER
BY- MAYUR PATEL

3. DELAYED PUBERTY
MENTAL
RETARDATION
SMALL STATURE
HYPOTONIA
HYPOGONADISM
SMALL HAND, FEET
OBESITY
PRADER WILLI
SYNDROME
MENTAL
RETARDATION
POLYDACTYLY
RETINITIS
PIGMENTOSA
OBESITY
LAURENCE MOON
BIEDL SYNDROME
GENITAL HYPOPLASIA
OBESITY
HYPOGONADOTROPIC
HYPOGONADISM
FROHLICH
SYNDROME
Y CHROMOSOMAL
ABNORMALITY
NORMAL/ TALL
STATURE
SWAYER SYNDROME
BY- MAYUR PATEL

4. INCREASE RISK
OF INFECTION
Albinism
neuropathy
Chediak hegashi
ataxia
skin lession
(telangiectasia)
risk of Ca
Ataxia telangiectasia
(Louise bar syndrm)
thrombocytopenia
eczema
Wiscott aldrich
syndm
x linked
agammaglobulinemia
Bruton disease
BY- MAYUR PATEL