Excerpt from The Treasury of Human Inheritance<br/><br/>Generation. IV. 1  6, children of III. 2 and III. 3. The three sons had each one foot enlarged, the limbs of the three daughters being normal. The order of birth of these children is not stated. IV. 7 and IV. 8, the eight children of III. 4 and III. 5. One of the eight, a boy, has one enlarged foot, the other seven being normal, three of the seven are dead. IV. 9  IV. 14, the five children of III. 7 and III. 8, the youngest  sex rl  has an enlarged oedematous foot, the others being normal. IV. 15 and 16, the four children of III. 9 and III. 10. The youngest, sex not stated, has an oedematous leg. IV. 17, IV. 18, IV. 19, three children of III. 11 and III. 12. Only the boy, IV. 19, was affected and suffered from enlarged foot. When he reached maturity his testicles began to swell and progressed to such an extent that one of them had to be removed. Strange to say as the testicle increased in Size the oedematous foot decreased and after the operation became and remained normal. IV. 20 and IV. 21, children of III. 15. By her first husband the three children (sex not stated) were normal, whereas by her second husband she had a son, IV. 21, with great oedema of both feet and both legs up to the level of the knees. The left side was more oedematous however than the right. IV. 21, an American clergyman, was the patient who consulted Milroy and whose condition led to Milroy's enquiry into the family history. V. 1, 2, and 3, the 11 grandchildren of III. 2 and III. 3. Of them is stated that two, viz. A son and a daughter, were affected with the family disease. In both cases the foot alone on one side was affected. The respective parents of these children are not given. V. 4, nine grandchildren of III. 4 and III. 5, sex and order of birth not stated, none of them were oedematous. V. 5, V. 6, V. 7, nine grandchildren of III. 7 and III. 8. Their order of birth and in seven cases, V. 5, the sex not stated. V.
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Paperback. Zustand: New. Print on Demand. This book explores the fascinating and complex origins of human conditions and diseases through the study of family lineages, providing remarkable insights into the inheritance of traits. The author has compiled a collection of 161 cases of conditions such as chronic troedema, deaf-mutism, ability, hare lip, cleft palate, haemophilia, dwarfism, cataract, dental defects, and many more. By delving into the family histories of those affected, the book uncovers patterns of inheritance, shedding light on the connection between genetics and the development of various characteristics. This in-depth analysis not only expands our understanding of the role of heredity in human health and disease, but also paves the way for more personalized and effective approaches to healthcare in the future. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book. print-on-demand item. Bestandsnummer des Verkäufers 9781334685668_0
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