Brachydactyly
A syndrome of high phenotypic variability caused by contiguous gene deletions in 2q37. The inheritance is autosomal dominant. The condition may be characterized by brachydactly type E; mental retardation; short stature; and other skeletal, cardiovascular, and neurologic manifestations.
Disease Alternative Name
Self Employed. Now Doing My Practice
Pediatric Consultant
MKCG MCH
MBBS and MD (pediatrics)
Worked at Jalna.Latur. and Now Mumbai.
Consulting Surgeon
Consulting Surgeon.
M.S.,FICS,FAIS. Sr. Surgeon.
Super Specialist in Reproductive Endocrinology
Dr KUTE HOSPITAL
Dr KUTE HOSPITAL
Govt. Medical College Miraj
D M &S
SHANTI MEMORIAL HOSPITAL
CONSULTANT PEDIATRICIAN MD,DNB
IPGME&R
MD
Distt. Red Cross Society Bhawan
Honorary Medical Officer
SPMC, Bikaner
MBBS
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Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital anomaly of female urogenital tract involving combined anomaly of Mullerian & mesonephric ducts which includes a triad of didelphys uterus, obstructed hemivagina, & ipsilateral renal agenesis. Dr Sheetal Singh sharing here a Case Report on “Herlyn Werner Wunderlich Syndrome diagnosed in a pregnant woman”. Share your thoughts and insights.
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May Round 1 and 2. Quiz posted on 4th and 11th May 2024. Congratulations to all the top performers. Thank you all for your participation. Keep participating!
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Hypertension frequently coexists with diabetes, hyperlipidemia, or the metabolic syndrome etc. The identification and management of these risk factors is an important part of the overall management of hypertensive patients. In this learning series post which may be helping with the doctor community to revisit important Hypertension related treatment scenario & insights.
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