نتایج جستجو برای: congenital absence of skin

تعداد نتایج: 21198095  

  Pulmonary agenesis is a rare congenital anomaly in which there is absence of pulmonary parenchyma as well as its bold vessels. It is an unusual cause of respiratory distress in newborn. Unilateral agenesis of lung is often associated with other congenital anomalies. The condition may lead to diagnostic difficulties.   Right pulmonary agenesis has poor prognosis. Here we present a case of fem...

M Barzegari RM Robati SN Emadi

Congenital diffuse Melanosis is one of the rarest clinical manifestations of hereditary universal Melanosis and only few cases have been reported all over the world. The presented case is a 54-year-old man who presented to us complaining of erythematous annular lesions on his face and neck since 8 months ago. Diffuse pigmentation of his skin took our attention. According to the patient, d...

2016
Dror Paley

Tibial hemimelia is a rare congenital lower limb deficiency presenting with a wide spectrum of associated congenital anomalies, deficiencies and duplications. Reconstructive options have been limited, and the gold standard for treatment has remained amputation with prosthetic fitting. There is now a better understanding of the genetics, etiology and pathoanatomy of tibial hemimelia. Armed with ...

Journal: :Archives of Pediatrics & Adolescent Medicine 1921

Journal: :Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2008
Robert T Adelson Kian Karimi Nicholas Herrero

Introduction: Congenital defects of the nasal cartilaginous skeleton are rare, yet clinically relevant, entities that are important to recognize prior to operative repair Methods: A 47 year old woman was referred to our institution for lifelong leftsided nasal airway obstruction. On physical examination, a complete absence of the left lower lateral cartilage was suspected. Hypothesis: Complete ...

Journal: :Indian pediatrics 1995
M L Kulkarni C Sureshkumar V Venkataraman

Cryptophthalmos is the congenital absence of eyelid with skin passing continuously from the head to the cheeks over a malformed eye. The term cryptophthalmos was coined by Zehender and Manz in 1872, when they first described a patient with bilateral cryptophthalmos and multiple congenital anomalies(l). In 1962 Fraser described 4 cases of cryptophthalmos and multiple malformations in two sibship...

2011
Michael D. Fried

(1.2) the ranges of f and g are identical on almost all OK/p. The most trivial cases are where g(x) = f(ax + b) for some a, b ∈ Q̄, the algebraic numbers. When K = Q, mostly that relation forces a, b∈K. For example this holds when f is indecomposable (not a composite of lower degree polynomials). With the indecomposability assumption, solutions to Davenport’s and Schinzel’s problems were essenti...

Journal: :The hematology journal : the official journal of the European Haematology Association 2000
P K Hegarty B Tan R O'Sullivan C C Cronin M P Brady

INTRODUCTION Asplenia causes a deficiency in immunity with a long-term risk of fulminant infection, associated with significant mortality. Patient compliance requires an understanding of risks of infection and its prevention. The impact of patient education has been little studied. MATERIALS AND METHODS To ascertain the degree of knowledge held by patients who have undergone splenectomy, a co...

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