Introduction: Supernumerary nipples are common anomalies which may be associated with several systemic disorders, particularly urinary tract abnormalities. Case report: Here we report a case of a 4½ year old male presenting to the pediatric out patient clinic with fever for three days and recurrent sinopulmonary infections. The child had supernumerary nipples over the right side with deformed thoracic cage, congenital scoliosis, diastematomyelia, crossed renal ectopia, and spina bifida. All the conditions present together did not match any syndrome reported till date. Conclusion: This was a rare syndrome and did not match fully with any known syndromes till date. This case warranted further investigation for its definite diagn...
Congenital nephrotic syndrome (CNS) is a rare disorder characterized by massive proteinuria, hypoalb...
Supernumerary kidney is the rarest of all renal anomalies; fewer than 80 cases have been reported in...
Hypotonia-Cystinuria syndrome (HCS) is a rare disease, caused by a mutation in two contiguous genes ...
Supernumerary kidney (SNK) is a rare congenital anomaly with fewer than 100 cases reported in the En...
OBJECTIVE: Supernumerary nipples (SNN), or polythelia, are the most common form of the accessory m...
The frequency of accessory nipples in black Americans is almost eight times greater than in white Eu...
Polythelia is a congenital anomaly in which there is a third or more nipples. Although it is a relat...
Introduction: From asymptomatic ectopic kidneys to potentially fatal renal agenesis, congenital abno...
A high rate of association between supernumerary nipples (SNN) and genitourinary abnormalities has b...
A supernumerary nipple (SN), usually arises within the embryonic milk lines but can also occur in lo...
Renal ectopia is a rare anomaly which may occur due to an abnormal ascent of the kidney. It is usual...
AbstractThe triad of deficient abdominal wall musculature, undescended testes and urinary tract anom...
Introduction: The spectrum of congenital anomalies of the kidneys and the urinary tract is extremely...
Background: Poland syndrome (PS) is a rare congenital anomaly associated with absent or hypoplastic ...
We present here a rare case of Scimitar syndrome on a full-term newborn female issued from consangui...
Congenital nephrotic syndrome (CNS) is a rare disorder characterized by massive proteinuria, hypoalb...
Supernumerary kidney is the rarest of all renal anomalies; fewer than 80 cases have been reported in...
Hypotonia-Cystinuria syndrome (HCS) is a rare disease, caused by a mutation in two contiguous genes ...
Supernumerary kidney (SNK) is a rare congenital anomaly with fewer than 100 cases reported in the En...
OBJECTIVE: Supernumerary nipples (SNN), or polythelia, are the most common form of the accessory m...
The frequency of accessory nipples in black Americans is almost eight times greater than in white Eu...
Polythelia is a congenital anomaly in which there is a third or more nipples. Although it is a relat...
Introduction: From asymptomatic ectopic kidneys to potentially fatal renal agenesis, congenital abno...
A high rate of association between supernumerary nipples (SNN) and genitourinary abnormalities has b...
A supernumerary nipple (SN), usually arises within the embryonic milk lines but can also occur in lo...
Renal ectopia is a rare anomaly which may occur due to an abnormal ascent of the kidney. It is usual...
AbstractThe triad of deficient abdominal wall musculature, undescended testes and urinary tract anom...
Introduction: The spectrum of congenital anomalies of the kidneys and the urinary tract is extremely...
Background: Poland syndrome (PS) is a rare congenital anomaly associated with absent or hypoplastic ...
We present here a rare case of Scimitar syndrome on a full-term newborn female issued from consangui...
Congenital nephrotic syndrome (CNS) is a rare disorder characterized by massive proteinuria, hypoalb...
Supernumerary kidney is the rarest of all renal anomalies; fewer than 80 cases have been reported in...
Hypotonia-Cystinuria syndrome (HCS) is a rare disease, caused by a mutation in two contiguous genes ...