Ramon’s Syndrome: A Rare Entity
نویسندگان
چکیده
1Alexander, 2Sherry Peter, 3Sheela Nampoothiri, 4Latha Rao, 5Ajith Nambiar 4Ravi Veeraraghavan, 4Ushass Puthalath 1Professor, Department of Oral Medicine and Radiology, Amrita School of Dentistry, Kochi, Kerala, India 2Consultant, Head and Neck Institute, Amrita Institute of Medical Sciences, Kochi, Kerala, India 3Professor, Department of Pediatric Genetics, Amrita Institute of Medical Sciences, Kochi, Kerala, India 4Reader, Department of Oral and Maxillofacial Surgery, Amrita School of Dentistry, Kochi, Kerala, India 5Associate Professor, Department of Pathology, Amrita Institute of Medical Sciences, Kochi, Kerala, India
منابع مشابه
Robinow Syndrome: a Rare Case Report from a Tertiary Care Hospital in Eastern India
Background Robinow syndrome is a rare congenital disorder with phenotypically heterogeneous abnormalities. Two modes of inheritances are known for this syndrome namely autosomal recessive and autosomal dominant. Case Report We describe here an eighteen-month-old child who had mesomelic short stature, abnormal facial features, clinodactyly, micropenis and vertebral changes which were further sup...
متن کاملNeuromyelitis Optica in Children: A Rare Entity
Neuromyelitis optica (also known as Devic's disease or Devic's syndrome) is an uncommon disorder in pediatric age group, and is characterized by acute or subacute optic neuritis and transverse myelitis. Here we report an 11- year- old female child with relapsing Neuromyelitis optica (NMO) confirmed by positive NMO- IgG antibody and had clinical recovery with high dose methyl prednisolone t...
متن کاملOrtner’s Syndrome-A Rare Cause of Hoarseness: Its Importance to an Otorhinolaryngologist
Introduction: Cardiovocal hoarseness (Ortner’s syndrome) is hoarseness of voice due to recurrent laryngeal nerve involvement secondary to cardiovascular disease. Recurrent laryngeal nerve in its course (especially the left side) follows a path that brings it in close proximity to numerous structures. These structures interfere with its function by pressure or by disruption of the nerve caused b...
متن کاملگزارش دو مورد بیمار مبتلا به سندرم راد
Rud syndrome is a rare disease entity that consists of congenital ichthyosis, mental retardation, hypogonadism, and epilepsy. In this article two cases that are sibling are reported. The parents are relative. The elder one who is a 16-yr old female suffers from sever ichthyosis, hypocalcemic tetany, sever mental and grown retardation, and hypogonadism. In the second patient a 9-yr old male the ...
متن کاملNecrotizing Sialometaplasia of the Larynx: A Rare Entity Obscuring a Malignancy
Introduction: Necrotizing sialometaplasia is a rare, benign, and self-limiting inflammatory lesion that commonly involves minor salivary glands. It is theoretically associated with ischemia. It is commonly found in the palate, and laryngeal presentation is a very unusual entity. Almost half of such cases have an underlying malignancy; therefore, suspicion of a malignant lesion should be high wh...
متن کامل